Triazine derivatives as UV absorbers

ABSTRACT

The present invention relates to new compounds of formula (I), wherein R1, R2, R3, R4, R5, R6, R7, and R8 independently from each other are hydrogen; C1-C18alkyl; C2-C18alkenyl; C5-C7, cycloalkyl; C1-C6alkylene-C5-C7, cycloalkyl; R9 is hydrogen; C1-C18alkyl; C2-C18alkenyl; C5-C7cycloalkyl; C1-C6alkylene-C5-C7cycloalkyl; C6-C10aryl; A is —S—; —O— or —NR10—, wherein R10 has the same meanings as R9; X is COOR11; CONR12R13; SO3, R14; or SO2NR15R16, wherein R11, R12, R13, R14, R15, and R16, have independently from each other the same meanings as R9; to their preparation and to their use as UV absorbers in cosmetic and pharmaceutical formulations.

The present invention relates to anisyl-bis(arylamino)-triazines, to the preparation of these compounds and to their use as UV absorbers in cosmetic and pharmaceutical formulations.

Depending on their wavelength, UV rays are divided in UV-A rays (320-400 nm) and UV-B rays (280-320 nm). The harmful effect, in particular the occurrence of sunburn (erythema), increases not only with the duration of exposure but also with decreasing wavelength and is thus significantly more strongly marked in the case of UV-B radiation than in the case of UV-A radiation. Since erythemas can occur even after short exposure to the sun, in some cases after 20-30 minutes, efficient protection against this radiation is of particular importance.

Ultra violet light absorbing compounds (UV-absorbers) do not absorb the complete spectrum of ultra violet light to the same extent at each wavelength. Characteristics of UV-absorbers are therefore the wavelength at which absorption is largest (in nm), and the absorption percentage at this wavelength (relative, calculated using the law of Lambert-Beer). Both this wavelength and absorption percentage at maximum absorbency can be influenced by other components present together with the UV-absorber.

It was now found that specific anisyl-bis(arylamino)-triazines are very effective UV absorbers.

Therefore, the present invention relates to compounds of formula

-   R₁, R₂, R₃, R₄, R₅, R₆, R₇ and R₈ independently from each other are     hydrogen; C₁-C₁₈alkyl; C₂-C₁₈alkenyl; C₅-C₇cycloalkyl; or     C₁-C₆alkylene-C₅-C₇cycloalkyl; -   R₉ is hydrogen; C₁-C₁₈alkyl; C₂-C₁₈alkenyl; C₅-C₇cycloalkyl;     C₁-C₆alkylene-C₅-C₇cycloalkyl; or C₆-C₁₀aryl; -   A is —S—; —O— or —NR₁₀—, wherein R₁₀ has the same meanings as R₉; -   X is COOR₁₁; CONR₁₂R₁₃; SO₃R₁₄; or SO₂NR₁₅R₁₆, wherein R₁₁, R₁₂,     R₁₃, R₁₄, R₁₅ and R₁₆ have independently from each other the same     meanings as R₉.

C₁-C₁₈alkyl denotes straight-chain and branched hydrocarbon radicals, for example methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, 2-ethylbutyl, n-pentyl, isopentyl, 1-methylpentyl, 1,3-dimethylbutyl, n-hexyl, 1-methylhexyl, n-heptyl, isoheptyl, 1,1,3,3-tetra-methylbutyl, 1-methylheptyl, 3-methylheptyl, n-octyl, 2-ethylhexyl, 1,1,3-tri-methylhexyl, 1,1,3,3-tetramethylpentyl, nonyl, decyl, undecyl, 1-methylundecyl, dodecyl, tridecyl, tetradecyl, pentadecyl or hexadecyl or octadecyl.

C₁-C₁₈alkyl may be mono- or poly substituted by C₁-C₄-alkyl, halogen, CN, COOH, COOC₁-C₄-alkyl, O—C₁-C₄-alkyl, NH₂ or NO₂.

C₂-C₁₈alkenyl is for example, allyl, methallyl, isopropenyl, 2-butenyl, 3-butenyl, isobutenyl, n-penta-2,4-dienyl, 3-methyl-but-2-enyl, n-oct-2-enyl, n-dodec-2-enyl, isododecenyl, n-dodec-2-enyl or n-octadec-4-enyl.

C₂-C₁₈alkenyl may be mono- or poly substituted by C₁-C₄-alkyl, halogen, CN, COOH, COOC₁-C₄-alkyl, O—C₁-C₄-alkyl, NH₂ or NO₂.

C₅-C₇cycloalkyl may be mono- or poly substituted by C₁-C₄-alkyl, halogen, CN, COOH, COOC₁-C₄-alkyl, O—C₁-C₄-alkyl, NH₂ or NO₂.

C₆-C₁₀aryl is, for example, phenyl or naphthyl.

Preferred embodiments of the present invention are compounds of formula (1), wherein R₁, R₂, R₃, R₄, R₅, R₆, R₇ and R₈ independently from each other are hydrogen; C₁-C₁₀alkyl;

-   C₂-C₁₀alkenyl; C₅-C₇cycloalkyl; or C₁-C₄alkylene-C₅-C₇cycloalkyl; -   R₉ is hydrogen; C₁-C₁₀alkyl; C₂-C₁₀alkenyl; C₅-C₇cycloalkyl;     C₁-C₄alkylene-C₅-C₇cycloalkyl; naphthyl; or phenyl -   A is —S—; —O— or —NR₁₀—, wherein R₁₀ has the same meanings as R₉; -   X is COOR₁₁; CONR₁₂R₁₃; SO₃R₁₄ or SO₂NR₁₅R₁₆, wherein R₁₁, R₁₂, R₁₃,     R₁₄, R₁₅ and R₁₆ have independently from each other the same     meanings as R₉.

Mostly preferred are compounds of formula (1), wherein

R₁, R₂, R₃, R₄, R₅, R₆, R₇ and R₈ are hydrogen; and

X, R₉ and R₁₀ are defined as in formula (1).

Of preferred interest are compounds of formula (1), wherein

R₁₁, R₁₂, R₁₃, R₁₄, R₁₅ and R₁₆ are hydrogen; or C₁-C₁₂alkyl; and

R₁, R₂, R₃, R₄, R₅, R₆, R₇, R₈, R₉, R₁₀ and X are defined as in formula (1), and most preferably compounds of formula (1), wherein

R₁, R₂, R₃, R₄, R₅, R₆, R₇ R₈, are hydrogen;

R₉, R₁₀, R₁₁, R₁₂, R₁₃, R₁₄, R₁₅, and R₁₆ are hydrogen; or C₁-C₁₂alkyl; and

X is defined as in formula (1).

More preferred embodiments are compounds of formula

R₉, A and X have the same meanings as defined in formula (1).

Of special interest are compounds of formula

wherein R₉ is C₁-C₅alkyl; and R₁₇ is hydrogen; C₁-C₁₂alkyl; or —NH₂.

A further embodiment of the present invention is a process for the preparation of compounds of formula (1), characterized in that one mol of at least one compound of formula

R₁, R₂, R₃, R₄ and R₉ have independently from each other the same meanings as defined in formula (1) and formula (2) and Y is halogen, preferably Cl, is reacted with at least two mols of at least one compound of formula

R₅, R₆, R₇, R₈, A and X have independently from each other the same meanings as defined in formula (1) and formula (2).

The reaction is preferably carried out in an inert solvent, for example dioxan.

The reaction temperature is preferably from 50 to 100° C., more preferably from 60 to 90° C.

The obtained reaction product is purified by conventional methods, such as for example recrystallisation.

The compounds of the formula (1) according to the present invention are particularly suitable as UV filters, i.e. for protecting ultraviolet-sensitive organic materials, in particular the skin and hair of humans and animals, from the harmful effects of UV radiation. These compounds are therefore suitable as sunscreens in cosmetic, pharmaceutical and veterinary medical preparations. These compounds can be used both in dissolved form and in the micronized state.

The UV absorbers according to the present invention can be used either in the dissolved state (soluble organic filters, solubelized organic filters) or in the micronised state (nanoscalar organic filters, particulate organic filters, UV-absorber pigments).

Any known process suitable for the preparation of microparticles can be used for the preparation of the micronised UV absorbers, for example:

-   -   wet-milling (low viscous micronisation process for pump-able         dispersions), with a hard grinding medium, for example zirconium         silicate balls in a ball mill and a protective surfactant or a         protective polymer in water or in a suitable organic solvent;     -   wet-kneading (high viscous micronisation process non pump-able         pastes) using a continuous or discontinuous (batch) kneader. For         a wet-kneading process a solvent (water or cosmetically         acceptable oils), a grinding-aid (surfactant, emulsifier) and a         polymeric grinding aid may be used.     -   Both processes may be used respectively     -   spray-drying from a suitable solvent, for example aqueous         suspensions or suspensions containing organic solvents, or true         solutions in water, ethanol, dichloroethane, toluene or         N-methylpyrrolidone etc.     -   by the expansion according to the RESS process (Rapid Expansion         of Supercritical Solutions) of supercritical fluids (e.g. CO₂)         in which the UV filter or filters is/are dissolved, or the         expansion of fluid carbon dioxide together with a solution of         one or more UV filters in a suitable organic solvent;     -   by reprecipitation from suitable solvents, including         supercritical fluids (GASR process=Gas Anti-Solvent         Recrystallisation/PCA process=Precipitation with Compressed         Anti-solvents).

As milling apparatus for the preparation of the micronised organic UV absorbers there may be used, for example, a jet mill, ball mill, vibratory mill or hammer mill, preferably a high-speed mixing mill. Even more preferably mills are modern ball mills, manufactures of these mill-types are for example Netzsch (LMZ-mill), Drais (DCP-viscoflow or cosmo), Buihler AG (centrifugal mills) or Bachhofer. The grinding is preferably carried out with a grinding aid. As kneading apparatus for the preparation of the micronised organic UV absorbers examples are typical sigma-hook batch kneaders but also serial batch kneaders (IKA-Werke) or continuous kneaders (Contiuna from Werner und Pfleiderer).

Useful low molecular weight grinding aids for all the above micronizing processes are surfactants and emulsifies as disclosed below in the chapters “emulsifiers” and “surfactants”.

Useful polymeric grinding aids for water dispersion are cosmetically acceptable water soluble Polymers with Mw>5000 g/mol for example: Acrylates (Salcare types), modified or non-modified polysaccharides, polyglucosides or xanthan gum. Furthermore an alkylated vinylpyrrolidone polymer, a vinylpyrrolidone/vinyl acetate copolymer, an acyl glutamate, an alkyl polyglucoside, ceteareth-25 or a phospholipid may be used. Oil dispersions may contain cosmetically acceptable waxy polymers or natural waxes as polymeric grinding aid to adjust viscosity during and after processing.

Useful solvents are water, brine, (poly-)ethylenglycol or glycerine for water-soluble dispersions and also cosmetically acceptable oils like described under “emollients” for oil-soluble dispersions.

The micronised UV absorbers so obtained usually have an average particle size from 0.02 to 2 micrometer, preferably from 0.05 to 1.5 micrometer and more especially from 0.1 to 1.0 micrometer.

The UV absorbers can also be used dry in powder form. For that purpose the UV absorbers are subjected to known grinding methods, such as vacuum atomization, countercurrent spray-drying etc. Such powders have a particle size of from 0.1 micrometer to 2 micro-meter.

To avoid the occurrence of agglomeration, the UV absorbers can be coated with a surface-active compound prior to the pulverisation process, for example with an anionic, non-ionic or amphoteric surfactant, e.g. a phospholipid or a known polymer, such as PVP, an acrylate etc.

The cosmetic formulations or pharmaceutical compositions according to the present invention can also contain one or more than one further UV filter as described in table 1-3.

The cosmetic or pharmaceutical preparations can be prepared by physically mixing the UV absorber(s) with the adjuvant using customary methods, for example by simply stirring together the individual components, especially by making use of the dissolution properties of already known cosmetic UV absorbers, for example octyl methoxy cinnamate, salicylic acid isooctyl ester, etc. The UV absorber can be used, for example, without further treatment, or in the micronised state, or in the form of a powder.

Cosmetic or pharmaceutical preparations contain from 0.0540% by weight, based on the total weight of the composition, of one UV absorber or UV absorber mixtures.

Preference is given to the use of mixing ratios of the UV absorber of formula (1) according to the invention and optionally further light-protective agents (as described in table 1-3) from 1:99 to 99:1, especially from 1:95 to 95:1 and preferably from 10:90 to 90:10, based on weight. Of special interest are mixing ratios of from 20:80 to 80:20, especially from 40:60 to 60:40 and preferably approximately 50:50. Such mixtures can be used, inter alia, to improve solubility or increase UV absorption.

The UV absorbers of formula (1) according to the present invention or combinations of UV filters are useful to protect skin, hair and/or natural or artificial hair color.

TABLE 1 Suitable UV filter substances which can be additionally used with the UV absorbers according to the present invention p-aminobenzoic acid derivatives, for example 4-dimethylaminobenzoic acid 2-ethylhexyl ester; salicylic acid derivatives, for example salicylic acid 2-ethylhexyl ester; benzophenone derivatives, for example 2-hydroxy-4-methoxybenzo- phenone and its 5-sulfonic acid derivative; dibenzoylmethane derivatives, for example 1-(4-tert-butylphenyl)-3- (4-methoxyphenyl)-propane-1,3-dione; diphenylacrylates, for example 2-ethylhexyl 2-cyano-3,3- diphenylacrylate, and 3-(benzofuranyl) 2-cyanoacrylate; 3-imidazol-4-ylacrylic acid and esters; benzofuran derivatives, especially 2-(p-aminophenyl)benzofuran derivatives, described in EP-A-582 189, US-A-5 338 539, US-A-5 518 713 and EP-A-613 893; polymeric UV absorbers, for example the benzylidene malonate derivatives described in EP-A-709 080; cinnamic acid derivatives, for example the 4-methoxycinnamic acid 2-ethylhexyl ester and isoamyl ester or cinnamic acid derivatives described in US-A-5 601 811 and WO 97/00851; camphor derivatives, for example 3-(4′-methyl)benzylidene-bornan-2-one, 3-benzylidene-bornan-2-one, N-[2(and 4)-2-oxyborn-3-ylidene- methyl)-benzyl]acrylamide polymer, 3-(4′-trimethylammonium)- benzylidene-bornan-2-one methyl sulfate, 3,3′-(1,4-phenylenedimethine)-bis(7,7-dimethyl-2- oxo-bicyclo[2.2.1]heptane-1-methanesulfonic acid) and salts, 3-(4′-sulfo)benzylidene-bornan-2-one and salts; camphorbenzalkonium methosulfate; hydroxyphenyltriazine compounds, for example 2-(4′-methoxyphenyl)- 4,6-bis(2′-hydroxy-4′-n-octyloxyphenyl)-1,3,5-triazine; 2,4-bis{[4-(3-(2-propyloxy)-2-hydroxy-propyloxy)-2- hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine; 2,4-bis{[4- (2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-[4-(2-methoxyethyl- carboxyl)-phenylamino]-1,3,5-triazine; 2,4-bis{[4- (tris(trimethylsilyloxy-silylpropyloxy)-2-hydroxy]-phenyl}- 6-(4-methoxyphenyl)-1,3,5-triazine; 2,4-bis{[4-(2″-methylpropenyloxy)- 2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine; 2,4-bis{[4-(1′,1′,1′,3′,5′,5′,5′-heptamethyltrisilyl-2″-methyl- propyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazine; 2,4-bis{[4-(3-(2-propyloxy)-2-hydroxy-propyloxy)-2- hydroxy]-phenyl}-6-[4-ethylcarboxy)-phenylamino]-1,3,5-triazine; benzotriazole compounds, for example 2,2′-methylene-bis(6- (2H-benzotriazol-2-yl)-4-(1,1,3,3-tetramethylbutyl)-phenol; trianilino-s-triazine derivatives, for example 2,4,6-trianiline-(p-carbo- 2′-ethyl-1′-oxy)-1,3,5-triazine and the UV absorbers disclosed in US-A-5 332 568, EP-A-517 104, EP-A-507 691, WO 93/17002 and EP-A-570 838; 2-phenylbenzimidazole-5-sulfonic acid and salts thereof; menthyl o-aminobenzoates; physical sunscreens coated or not as titanium dioxide, zinc oxide, iron oxides, mica, MnO, Fe₂O₃, Ce₂O₃, Al₂O₃, ZrO₂. (surface coatings: polymethylmethacrylate, methicone (methylhydrogenpolysiloxane as described in CAS 9004-73-3), dimethicone, isopropyl titanium triisostearate (as described in CAS 61417-49-0), metal soaps as magnesium stearate (as described in CAS 4086-70-8), perfluoroalcohol phosphate as C9-15 fluoroalcohol phosphate (as described in CAS 74499-44-8; JP 5-86984, JP 4-330007)). The primary particle size is an average of 15 nm-35 nm and the particle size in dispersion is in the range of 100 nm-300 nm. aminohydroxy-benzophenone derivatives disclosed in DE 10011317, EP 1133980 and EP 1046391 phenyl-benzimidazole derivatives as disclosed in EP 1167358 the UV absorbers described in “Sunscreens”, Eds. N. J. Lowe, N. A. Shaath, Marcel Dekker, Inc., New York and Basle or in Cosmetics & Toiletries (107), 50ff (1992) also can be used as additional UV protective substances.

TABLE 2 Suitable UV filter substances which can be additionally used with the UV absorbers according to the present invention are described in the following patents DE 100331804 Tab 1 p 4, tab 2 + 3 p 5 EP 613893 Ex 1-5 + 15, T 1, pp 6-8 EP 1000950 Comp. in table 1, pp 18-21 EP 1005855 T 3, p 13 EP 1008586 Ex 1-3, pp 13-15 EP 1008593 Ex 1-8, pp 4-5 EP 1027883 Compound VII, p 3 EP 1027883 Comp I-VI, p 3 EP 1028120 Ex 1-5, pp 5-13 EP 1059082 Ex 1; T 1, pp 9-11 EP 1060734 T 1-3, pp 11-14 EP 1064922 Compounds 1-34, pp 6-14 EP 1081140 Ex 1-9, pp 11-16 EP 1103549 Compounds 1-76, pp 39-51 EP 1108712 4,5-Dimorpholino-3-hydroxypyridazine EP 1123934 T 3, p 10 EP 1129695 Ex 1-7, pp 13-14 EP 1167359 Ex 1 p11 and ex 2 p 12 EP 420707 B1 Ex 3, p 13 (CAS Regno 80142-49-0) EP 503338 T 1, pp 9-10 EP 517103 Ex 3, 4, 9, 10 pp 6-7 EP 517104 Ex 1, T 1, pp 4-5; Ex 8, T 2, pp 6-8 EP 626950 all compounds EP 669323 Ex 1-3, p 5 EP 780382 Ex 1-11, pp 5-7 EP 823418 Ex 1-4, pp 7-8 EP 826361 T 1, pp 5-6 EP 832641 Ex 5 + 6 p 7; t 2, p 8 EP 832642 Ex 22, T 3 pp, 10-15; T 4, p 16 EP 852137 T 2, pp 41-46 EP 858318 T 1, p 6 EP 863145 Ex 1-11, pp 12-18 EP 895776 Comp. in rows 48-58, p 3; R 25 + 33, p 5 EP 911020 T 2, p 11-12 EP 916335 T 2-4, pp 19-41 EP 924246 T 2, p 9 EP 933376 Ex 1-15, pp 10-21 EP 944624 Ex 1 + 2, pp13-15 EP 945125 T 3 a + b, pp 14-15 EP 967200 Ex 2; T 3-5; pp 17-20 EP 969004 Ex 5, T 1, pp 6-8 JP 2000319629 CAS Regno. 80142-49-0, 137215-83-9, 307947-82-6 U.S. Pat. No. 5,635,343 all compounds on pp 5-10 U.S. Pat. No. 5,338,539 Ex 1-9, pp 3 + 4 U.S. Pat. No. 5,346,691 Ex 40, p 7; T 5, p 8 U.S. Pat. No. 5,801,244 Ex 1-5, pp 6-7 WO 0149686 Ex 1-5, pp 16-21 WO 0168047 Tables on pp 85-96 WO 0181297 Ex 1-3 pp 9-11 WO 0238537 All componds p 3, compounds on rows 1-10 p 4 WO 9217461 Ex 1-22, pp 10-20 WO 9220690 Polymeric comp in examples 3-6 WO 9301164 T 1 + 2, pp 13-22 WO 9714680 Ex 1-3, p 10 (Abbreviations T: table, R: row, Comp: compound, Ex: compound(s) of patent example, p: page)

TABLE 3 Suitable UV filter substances which can be additionally used with the UV absorbers according to the present invention No. Chemical Name CAS No. 1 (+/−)-1,7,7-trimethyl-3-[(4-methylphenyl)- 36861-47-9 methylene]-bicyclo-[2.2.1]heptan-2-one 2 1,7,7-trimethyl-3-(phenylmethylene)- 15087-24-8 bicyclo[2.2.1]heptan-2-one 3 (2-Hydroxy-4-methoxyphenyl)(4- 1641-17-4 methylphenyl)methanone 4 2,4-dihydroxybenzophenone 131-56-6 5 2,2′,4,4′-tetrahydroxybenzophenone 131-55-5 6 2-Hydroxy-4-methoxy benzophenone; 131-57-7 7 2-Hydroxy-4-methoxy benzophenone- 4065-45-6 5-sulfonic acid 8 2,2′-dihydroxy-4,4′-dimethoxybenzophenone 131-54-4 9 2,2′-Dihydroxy-4-methoxybenzophenone 131-53-3 10 Alpha-(2-oxoborn-3-ylidene)toluene- 56039-58-8 4-sulphonic acid and its salts 11 1-[4-(1,1-dimethylethyl)phenyl]-3-(4- 70356-09-1 methoxyphenyl)propane-1,3-dione 12 Methyl N,N,N-trimethyl-4-[(4,7,7-trimethyl-3- 52793-97-2 oxobicyclo[2,2,1]hept-2-ylidene)methyl]- anilinium sulphate; 22 3,3,5-Trimethyl cyclohexyl-2-hydroxy benzoate 118-56-9 23 Isopentyl p-methoxycinnamate 71617-10-2 27 Menthyl-o-aminobenzoate 134-09-8 28 Menthyl salicylate 89-46-3 29 2-Ethylhexyl 2-cyano,3,3-diphenylacrylate 6197-30-4 30 2-ethylhexyl 4-(dimethylamino)benzoate 21245-02-3 31 2-ethylhexyl 4-methoxycinnamate 5466-77-3 32 2-ethylhexyl salicylate 118-60-5 33 Benzoic acid, 4,4′,4″-(1,3,5-triazine- 88122-99-0 2,4,6-triyltriimino)tris-, tris(2-ethylhexyl) ester; 2,4,6-Trianilino- (p-carbo-2′-ethylhexyl-1′-oxi)-1,3,5-triazine 34 4-aminobenzoic acid 150-13-0 35 Benzoic acid, 4-amino-, ethyl ester, 113010-52-9 polymer with oxirane 38 2-phenyl-1H-benzimidazole-5-sulphonic acid 27503-81-7 39 2-Propenamide, N-[[4-[(4,7,7- 147897-12-9 trimethyl-3-oxobicyclo[2.2.1]hept-2- ylidene)methyl]phenyl]methyl]-, homopolymer 1 (+/−)-1,7,7-trimethyl-3-[(4-methylphenyl)- 36861-47-9 methylene]-[bicyclo-2.2.1]heptan-2-one 40 Triethanolamine salicylate 2174-16-5 41 3,3′-(1,4-phenylenedimethylene)bis[7,7- 90457-82-2 dimethyl-2-oxo-bicyclo[2.2.1]heptane- 1-methanesulfonic acid] 42 Titanium dioxide 13463-67-7 44 Zinc oxide 1314-13-2 45 2,2′-Methylene-bis-[6-(2H-benzotriazol-2-yl)-4- 103597-45-1 (1,1,3,3-tetramethyl-butyl)-phenol] 46 2,4-bis{[4-(2-ethylhexyloxy)-2-hydroxy]- 187393-00-6 phenyl}-6-(4-methoxyphenyl)-(1,3,5)-triazine 47 1H-Benzimidazole-4,6-disulfonic acid, 2,2′-(1,4- 180898-37-7 phenylene)bis-, disodium salt 48 Benzoic acid, 4,4′-[[6-[[4-[[(1,1-dimethylethyl)- 154702-15-5 amino]carbonyl]phenyl]amino]1,3,5-triazine- 2,4-diyl]diimino]bis-, bis(2-ethylhexyl)ester 49 Phenol, 2-(2H-benzotriazol-2-yl)-4-methyl- 155633-54-8 6-[2-methyl-3-[1,3,3,3-tetramethyl- 1-[(trimethylsilyl)oxy]disiloxanyl]propyl]- 50 alpha-(trimethylsilyl)-omega-(trimethyl- 207574-74-1 silyloxy)poly[oxy(dimethyl)-silylene]-co- [oxy(methyl)(2-{p-[2,2-bis(ethoxycarbonyl)- vinyl]-phenoxy}-1methyleneethyl)silylene]-co- [oxy(methyl)-(2-{p-[2,2-bis(ethoxycarbonyl)- vinyl]phenoxy}-prop-1-enyl)silylene] 51 Benzenesulfonic acid, 3-(2H-benzotriazol- 92484-48-5 2-yl)-4-hydroxy-5-(1-methylpropyl)-, monosodium salt 52 Benzoic acid, 2-[4-(diethylamino)-2- 302776-68-7 hydroxybenzoyl]-, hexyl ester 53 1-Dodecanaminium, N-[3-[[4-(dimethylamino)- 156679-41-3 benzoyl]amino]-propyl]N,N-dimethyl-, salt with 4-methylbenzenesulfonic acid (1:1) 54 1-Propanaminium, N,N,N-trimethyl-3-[(1-oxo- 177190-98-6 3-phenyl-2-propenyl)-amino]-, chloride 55 1H-Benzimidazole-4,6-disulfonic acid, 170864-82-1 2,2′-(1,4-phenylene)bis- 56 1,3,5-Triazine, 2,4,6-tris(4-methoxyphenyl)- 7753-12-0 57 1,3,5-Triazine, 2,4,6-tris[4-[(2- 208114-14-1 ethylhexyl)oxy]phenyl]- 58 1-Propanaminium, 3-[[3-[3-(2H-benzotriazol-2- 340964-15-0 yl)-5-(1,1-dimethylethyl)-4-hydroxyphenyl]-1- oxopropyl]-amino]-N,N-diethyl-N-methyl-, methyl sulfate (salt) 59 2-Propenoic acid, 3-(1H-imidazol-4-yl)- 104-98-3 60 Benzoic acid, 2-hydroxy-, [4-(1- 94134-93-7 methylethyl)phenyl]methyl ester 61 1,2,3-Propanetriol, 1-(4-aminobenzoate) 136-44-7 62 Benzeneacetic acid, 3,4-dimethoxy-a-oxo- 4732-70-1 63 2-Propenoic acid, 2-cyano-3,3-diphenyl-, 5232-99-5 ethyl ester

Suitable UV filter substances which can be additionally used with the UV absorbers according to the present invention are any UV-A and UV-B filter substances.

The cosmetic or pharmaceutical preparations may be, for example, creams, gels, lotions, alcoholic and aqueous/alcoholic solutions, emulsions, wax/fat compositions, stick preparations, powders or ointments. In addition to the above mentioned UV filters, the cosmetic or pharmaceutical preparations may contain further adjuvants as described below.

As water- and oil-containing emulsions (e.g. W/O, O/W, O/W/O and W/O/W emulsions or microemulsions) the preparations contain, for example, from 0.1 to 30% by weight, preferably from 0.1 to 15% by weight and especially from 0.5 to 10% by weight, based on the total weight of the composition, of one or more UV absorbers, from 1 to 60% by weight, especially from 5 to 50% by weight and preferably from 10 to 35% by weight, based on the total weight of the composition, of at least one oil component, from 0 to 30% by weight, especially from 1 to 30% by weight und preferably from 4 to 20% by weight, based on the total weight of the composition, of at least one emulsifier, from 10 to 90% by weight, especially from 30 to 90% by weight, based on the total weight of the composition, of water, and from 0 to 88.9% by weight, especially from 1 to 50% by weight, of further cosmetically acceptable adjuvants.

The cosmetic or pharmaceutical compositions/preparations according to the invention may also contain one or one more additional compounds as described below.

Fatty Alcohols

Guerbet alcohols based on fatty alcohols having from 6 to 18, preferably from 8 to 10 carbon atoms including cetyl alcohol, stearyl alcohol, cetearyl alcohol, oleyl alcohol, octyldodecanol, benzoate of C12-C15 alcohols, acetylated lanolin alcohol, etc.

Esters of Fatty Acids

Esters of linear C₆-C₂₄ fatty acids with linear C₃-C₂₄ alcohols, esters of branched C₆-C₁₃carboxylic acids with linear C₆-C₂₄ fatty alcohols, esters of linear C₆-C₂₄ fatty acids with branched alcohols, especially 2-ethylhexanol, esters of hydroxycarboxylic acids with linear or branched C₆-C₂₂ fatty alcohols, especially dioctyl malates, esters of linear and/or branched fatty acids with polyhydric alcohols (for example propylene glycol, dimer diol or trimer triol) and/or Guerbet alcohols, for example caproic acid, caprylic acid, 2-ethylhexanoic acid, capric acid, lauric acid, isotridecanoic acid, myristic acid, palmitic acid, palmitoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, elaeostearic acid, arachidic acid, gadoleic acid, behenic acid and erucic acid and technical-grade mixtures thereof (obtained, for example, in the pressure removal of natural fats and oils, in the reduction of aldehydes from Roelen's oxosynthesis or in the dimerisation of unsaturated fatty acids) with alcohols, for example, isopropyl alcohol, caproic alcohol, capryl alcohol, 2-ethylhexyl alcohol, capric alcohol, lauryl alcohol, isotridecyl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, linoyl alcohol, linolenyl alcohol, elaeostearyl alcohol, arachidyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol and brassidyl alcohol and technical-grade mixtures thereof (obtained, for example, in the high-pressure hydrogenation of technical-grade methyl esters based on fats and oils or aldehydes from Roelen's oxosynthesis and as monomer fractions in the dimerisation of unsaturated fatty alcohols).

Examples of such ester oils are isopropylmyristate, isopropylpalmitate, isopropylstearate, isopropyl isostearate, isopropyloleate, n-butylstearate, n-hexyllaurate, n-decyloleate, isooctylstearate, iso-nonylstearate, isononyl isononanoate, 2-ethylhexylpalmitate, 2-hexyllaurate, 2-hexyldecylstearate, 2-octyldodecylpalmitate, oleyloleate, oleylerucate, erucyloleate, erucylerucate, cetearyl octanoate, cetyl palmitate, cetyl stearate, cetyl oleate, cetyl behenate, cetyl acetate, myristyl myristate, myristyl behenate, myristyl oleate, myristyl stearate, myristyl palmitate, myristyl lactate, propylene glycol dicaprylate/caprate, stearyl heptanoate, diisostearyl malate, octyl hydroxystearate, etc.

Other Adjuvants

diethylhexyl 2,6-naphthalate, di-n-butyl adipate, di(2-ethylhexyl)-adipate, di(2-ethylhexyl)-succinate and diisotridecyl acelaat, and also diol esters, such as ethylene glycol dioleate, ethylene glycol diisotridecanoate, propylene glycol di(2-ethylhexanoate), propylene glycol diisostearate, propylene glycol dipelargonate, butanediol diisostearate and neopentyl glycol dicaprylate. Esters of C₆-C₂₄ fatty alcohols and/or Guerbet alcohols with aromatic carboxylic acids, saturated and/or unsaturated, especially benzoic acid, esters of C₂-C₁₂dicarboxylic acids with linear or branched alcohols having from 1 to 22 carbon atoms or polyols having from 2 to 10 carbon atoms and from 2 to 6 hydroxy groups.

Natural or Synthetic Triglycerides Including Glyceryl Esters and Derivatives

Di- or tri-glycerides, based on C₆-C₁₈ fatty acids, modified by reaction with other alcohols (caprylic/capric triglyceride, wheat germ glycerides, etc.). Fatty acid esters of polyglycerin (polyglyceryl-n such as polyglyceryl-4 caprate, polyglyceryl-2 isostearate, etc. or castor oil, hydrogenated vegetable oil, sweet almond oil, wheat germ oil, sesame oil, hydrogenated cottonseed oil, coconut oil, avocado oil, corn oil, hydrogenated castor oil, shea butter, cocoa butter, soybean oil, mink oil, sunflower oil, safflower oil, macadamia nut oil, olive oil, hydrogenated tallow, apricot kernel oil, hazelnut oil, borago oil, etc.

Waxes including esters of long-chain acids and alcohols as well as compounds having wax-like properties, e.g., carnauba wax, beeswax (white or yellow), lanolin wax, candellila wax, ozokerite, japan wax, paraffin wax, microcrystalline wax, ceresin, cetearyl esters wax, synthetic beeswax, etc. Also, hydrophilic waxes as Cetearyl Alcohol or partial glycerides.

Pearlescent Waxes:

Ikylene glycol esters, especially ethylene glycol distearate; fatty acid alkanolamides, especially coco fatty acid diethanolamide; partial glycerides, especially stearic acid monoglyceride; esters of polyvalent, unsubstituted or hydroxy-substituted carboxylic acids with fatty alcohols having from 6 to 22 carbon atoms, especially long-chained esters of tartaric acid; fatty substances, for example fatty alcohols, fatty ketones, fatty aldehydes, fatty ethers and fatty carbonates, which in total have at least 24 carbon atoms, especially laurone and distearyl ether; fatty acids, such as stearic acid, hydroxystearic acid or behenic acid, ring-opening products of olefin epoxides having from 12 to 22 carbon atoms with fatty alcohols having from 12 to 22 carbon atoms and/or polyols having from 2 to 15 carbon atoms and from 2 to 10 hydroxy groups, and mixtures thereof.

Hydrocarbon Oils:

Mineral oil (light or heavy), petrolatum (yellow or white), microcrystalline wax, paraffinic and isoparaffinic compounds, hydrogenated isoparaffinic molecules as polydecenes and polybutene, hydrogenated polyisobutene, squalane, isohexadecane, isododecane and others from plant and animal kingdom.

Silicones or Siloxanes (Organosubstituted Polysiloxanes)

Dimethylpolysiloxanes, methylphenylpolysiloxanes, cyclic silicones, and also amino-, fatty acid-, alcohol-, polyether-, epoxy-, fluorine-, glycoside- and/or alkyl-modified silicone compounds, which at room temperature may be in either liquid or resinous form. Linear polysiloxanes, dimethicone (Dow Corning 200 fluid, Rhodia Mirasil DM), dimethiconol, cyclic silicone fluids, cyclopentasiloxanes volatiles (Dow Corning 345 fluid), phenyltrimethicone (Dow Corning 556 fluid). Also suitable are simethicones, which are mixtures of dimethicones having an average chain length of from 200 to 300 dimethylsiloxane units with hydrogenated silicates. A detailed survey by Todd et al. of suitable volatile silicones may in addition be found in Cosm. Toil. 91, 27 (1976).

Fluorinated or Perfluorinated Oils

Perfluorhexane, dimethylcyclohexane, ethylcyclopentane, polyperfluoromethylisopropyl ether.

Emulsifiers

Any conventionally usable emulsifier can be used for the compositions. Emulsifier systems may comprise for example: carboxylic acids and their salts: alcalin soap of sodium, potassium and ammonium, metallic soap of calcium or magnesium, organic basis soap such as Lauric, palmitic, stearic and oleic acid etc. . . . Allyl phosphates or phosphoric acid esters, acid phosphate, diethanolamine phosphate, potassium cetyl phosphate. Ethoxylated carboxylic acids or polyethyleneglycol esters, PEG-n acylates. Linear fatty alcohols having from 8 to 22 carbon atoms, branched from 2 to 30 mol of ethylene oxide and/or from 0 to 5 mol propylene oxide with fatty acids having from 12 to 22 carbon atoms and with alkylphenols having from 8 to 15 carbon atoms in the alkyl group. Fatty alcohol polyglycolether such as laureth-n, ceteareth-n, steareth-n, oleth-n. Fatty acid polyglycolether such as PEG-n stearate, PEG-n oleate, PEG-n cocoate. Monoglycerides and polyol esters. C12-C22 fatty acid mono- and diesters of addition products of from 1 to 30 mol of ethylene oxide with polyols. Fatty acid and polyglycerol ester such as monostearate glycerol, diisostearoyl polyglyceryl-3-diisostearates, polyglyceryl-3-diisostearates, triglyceryl diisostearates, polyglyceryl-2-sesquiisostearates or polyglyceryl dimerates. Mixtures of compounds from a plurality of those substance classes are also suitable. Fatty acid polyglycolesters such as monostearate diethylene glycol, fatty acid and polyethylene glycol esters, fatty acid and saccharose esters such as sucro esters, glycerol and saccharose esters such as sucro glycerides. Sorbitol and sorbitan, sorbitan mono- and di-esters of saturated and unsaturated fatty acids having from 6 to 22 carbon atoms and ethylene oxide addition products. Polysorbate-n series, sorbitan esters such as sesquilsostearate, sorbitan, PEG-(6)-isostearate sorbitan, PEG-(10)-sorbitan laurate, PEG-17-dioleate sorbitan. Glucose derivatives, C8-C22 alkyl-mono and oligo-glycosides and ethoxylated analogues with glucose being preferred as the sugar component. O/W emulsifiers such as methyl gluceth-20 sesquistearate, sorbitan stearate/sucrose cocoate, methyl glucose sesquistearate, cetearyl alcohol/cetearyl glucoside. W/O emulsifiers such as methyl glucose dioleate/methyl glucose isostearate. Sulfates and sulfonated derivatives, diallcylsulfosuccinates, dioctyl succinate, alleyl lauryl sulfonate, linear sulfonated parafins, sulfonated tetraproplyne sulfonate, sodium lauryl sulfates, amonium and ethanolamine lauryl sulfates, lauyl ether sulfates, sodium laureth sulfates, sulfosuccinates, aceyl isothionates, alkanolamide sulfates, taurines, methyl taurines, imidazole sulfates. Amine derivatives, amine salts, ethoxylated amines, oxide amine with chains containing an heterocycle such as alkyl imidazolines, pyridine derivatives, isoquinoteines, cetyl pyridinium chlorure, cetyl pyridinium bromide, quaternary ammonium such as cetyltrimethylbroide amonium broide (CTBA), stearyl-alkonium. Amide derivatives, alkanolamides such as acylamide DEA, ethoxylated amides such as PEG-n acylamide, oxydeamide. Polysiloxane/polyalkyl/polyether copolymers and derivatives, dimethicone, copolyols, silicone polyethylene oxide copolymer, silicone glycol copolymer. Propoxylated or POE-n ethers (Meroxapols), Polaxamers or poly(oxyethylene)_(m)-block-poly(oxypropylene)_(n)-block (oxyethylene). Zwitterionic surfactants that carry at least one quaternary ammonium group and at least one carboxylate and/or sulfonate group in the molecule. Zwitterionic surfactants that are especially suitable are betaines, such as N-alkyl-N,N-dimethylammonium glycinates, cocoalltyidimethylammonium glycinate, N-acylamino-propyl-N,N-dimethylammonium glycinates, cocoacylaminopropyldimethylammonium glycinate and 2-alkyl-3-carboxymethyl-3-hydroxyethylimidazolines each having from 8 to 18 carbon atoms in the alkyl or acyl group and also cocoacylaminoethylhydroxyethylcarboxymethylglycinate, N-alkylbetaine, N-alkylaminobetaines. Alkylimidazolines, alkylopeptides, lipoaminoacides, self emulsifying bases and the compounds as described in K. F. DePolo, A short textbook of cosmetology, Chapter 8, Table 8-7, p 250-251.

Non ionic bases such as PEG-6 beeswax (and) PEG-6 stearate (and) polyglyceryl-2-iso-stearate [Apifac], glyceryl stearate (and) PEG-100 stearate. [Arlacel 165], PEG-5 glyceryl stearate [arlatone 983 S], sorbitan oleate (and) polyglyceryl-3 ricinoleate. [Arlacel 1689], sorbitan stearate and sucrose cocoate [arlatone 2121], glyceryl stearate and laureth-23 [Cerasynth 945], cetearyl alcohol and ceteth-20 [Cetomacrogol Wax], cetearyl alcohol and colysorbate 60 and PEG-150 and stearate-20[Polawax GP 200, Polawax NF], cetearyl alcohol and cetearyl polyglucoside [Emulgade PL 1618], cetearyl alcohol and ceteareth-20 [Emulgade 1000NI, Cosmowax], cetearyl alcohol and PEG40 castor oil [Emulgade F Special], cetearyl alcohol and PEG40 castor oil and sodium cetearyl sulfate [Emulgade F], stearyl alcohol and steareth-7 and steareth-10 [Emulgator E 2155], cetearyl alcohol and szeareth-7 and steareth-10 [Emulsifying wax U.S.N.F], glyceryl stearate and PEG-75 stearate [Gelot 64], propylene glycol ceteth-3 acetate. [Hetester PCS], propylene glycol isoceth-3 acetate [Hetester PHA], cetearyl alcohol and ceteth-12 and oleth-12 [Lanbritol Wax N 21], PEG 6 stearate and PEG-32 stearate [Tefose 1500], PEG-6 stearate and ceteth-20 and steareth-20 [Tefose 2000], PEG-6 stearate and ceteth-20 and glyceryl stearate and steareth-20 [Tefose 2561], glyceryl stearate and ceteareth-20 [Teginacid H, C, X].

Anionic alkalin bases such as PEG-2 stearate SE, glyceryl stearate SE [Monelgine, Cutina KD], propylene glycol stearate [Tegin P]. Anionic acid bases such as cetearyl Alcohol and Sodium cetearyl sulfate [Lanette N, Cutina LE, Crodacol GP], cetearyl alcohol and sodium lauryl sulfate [Lanette W], trilaneth-4 phopshate and glycol stearate and PEG-2 stearate [Sedefos 75], glyceryl stearate and sodium lauryl Sulfate [Teginacid Special]. Cationic acid bases such as cetearyl alcohol and cetrimonium bromide.

The emulsifiers may be used in an amount of, for example, from 1 to 30% by weight, especially from 4 to 20% by weight and preferably from 5 to 10% by weight, based on the total weight of the composition.

When formulated in O/W emulsions, the preferably amount of such emulsifier system could represent 5% to 20% of the oil phase.

Adjuvants and Additives

The cosmetic/pharmaceutical preparations, for example creams, gels, lotions, alcoholic and aqueous/alcoholic solutions, emulsions, wax/fat compositions, stick preparations, powders or ointments, may in addition contain, as further adjuvants and additives, mild surfactants, super-fatting agents, consistency regulators, thickeners, polymers, stabilisers, biogenic active ingredients, deodorising active ingredients, anti-dandruff agents, film formers, swelling agents, further UV light-protective factors, antioxidants, hydrotropic agents, preservatives, insect repellents, self-tanning agents, solubilisers, perfume oils, colourants, bacteria-inhibiting agents and the like.

Super-Fatting Agents

Substances suitable for use as super-fatting agents are, for example, lanolin and lecithin and also polyethoxylated or acrylated lanolin and lecithin derivatives, polyol fatty acid esters, monoglycerides and fatty acid alkanolamides, the latter simultaneously acting as foam stabilisers.

Surfactants

Examples of suitable mild surfactants, that is to say surfactants especially well tolerated by the skin, include fatty alcohol polyglycol ether sulfates, monoglyceride sulfates, mono- and/or di-alkyl sulfosuccinates, fatty acid isethionates, fatty acid sarcosinates, fatty acid taurides, fatty acid glutamates, -olefin sulfonates, ethercarboxylic acids, alkyl oligoglucosides, fatty acid glucamides, alkylamidobetaines and/or protein fatty acid condensation products, the latter preferably being based on wheat proteins.

Consistency Regulators/Thickeners and Rheology Modifiers

Silicium dioxide, magnesium silicates, aluminium silicates, polysaccharides or derivatives thereof for example hyaluronic acid, xanthan gum, guar-guar, agar-agar, alginates, carraghenan, gellan, pectines, or modified cellulose such as hydroxycellulose, hydroxypropyl-methylcellulose. In addition polyacrylates or homopolymer of reticulated acrylic acids and polyacrylamides, carbomer (carbopol types 980, 981, 1382, ETD 2001, ETD2020, Ultrez 10) or Salcare range such as Salcare SC80(steareth-10 allyl ether/acrylates copolymer), Salcare SC81 (acrylates copolymer), Salcare SC91 and Salcare AST (sodium acrylates copolymer/PPG-1 trideceth-6), sepigel 305 (polyacrylamide/laureth-7), Simulgel NS and Simulgel EG (hydroxyethyl acrylate/sodium acryloyidimethyl taurate copolymer), Stabilen 30 (acrylates/vinyl isodecanoate crosspolymer), Pemulen TR-1 (acrylates/C10-30 alkyl acrylate crosspolymer), Luvigel EM (sodium acrylates copolymer), Aculyn 28 (acrylates/beheneth-25 methacrylate copolymer), etc.

Polymers

Suitable cationic polymers are, for example, cationic cellulose derivatives, for example a quaternised hydroxymethyl cellulose obtainable under the name Polymer JR 400 from Amerchol, cationic starches, copolymers of diallylammonium salts and acrylamides, quarternised vinylpyrrolidone/vinyl imidazole polymers, for example Luviquat® (BASF), condensation products of polyglycols and amines, quaternised collagen polypeptides, for example lauryl-dimonium hydroxypropyl hydrolyzed collagen (Lamequat®/Grünau), quaternised wheat polypeptides, polyethyleneimine, cationic silicone polymers, for example amidomethicones, copolymers of adipic acid and dimethylaminohydroxypropyldiethylenetriamine (Cartaretin/Sandoz), copolymers of acrylic acid with dimethyldiallylammonium chloride (Merquat 550/Chemviron), polyaminopolyamides, as described, for example, in FR-A-2 252 840, and the crosslinked water-soluble polymers thereof, cationic chitin derivatives, for example of quaternised chitosan, optionally distributed as microcrystals; condensation products of dihaloalkyls, for example dibromobutane, with bisdialkylamines, for example bisdimethylamino-1,3-propane, cationic guar gum, for example Jaguar C-17, Jaguar C-16 from Celanese, quaternised ammonium salt polymers, for example Mirapol A-15, Mirapol AD-1, Mirapol AZ-1 from Miranol. As anionic, zwitterionic, amphoteric and non-ionic polymers there come into consideration, for example, vinyl acetate/crotonic acid copolymers, vinylpyrrolidone/vinyl acrylate copolymers, vinyl acetate/butyl maleate/isobornyl acrylate copolymers, methyl vinyl ether/maleic anhydride copolymers and esters thereof, uncrosslinked polyacrylic acids and polyacrylic acids crosslinked with polyols, acrylamidopropyl-trimethyl-ammonium chloride/acrylate copolymers, octyl acrylamide/methyl methacrylate-tert-butylaminoethyl methacrylate/2-hydroxypropyl methacrylate copolymers, polyvinyl-pyrrolidone, vinylpyrrolidone/vinyl acetate copolymers, vinylpyrrolidone/dimethylaminoethyl methacrylate/vinyl caprolactam terpolymers and also optionally derivatised cellulose ethers and silicones. Furthermore the polymers as described in EP 1093796 (pages 3-8, paragraphs 17-68) may be used.

Biogenic Active Ingredients

Biogenic active ingredients are to be understood as meaning, for example, tocopherol, tocopherol acetate, tocopherol palmitate, ascorbic acid, deoxyribonucleic acid, retinol, bisabolol, allantoin, phytantriol, panthenol, AHA acids, amino acids, ceramides, pseudoceramides, essential oils, plant extracts and vitamin complexes.

Deodorising Active Ingredients

As deodorising active ingredients there come into consideration, for example, anti-perspirants, for example aluminium chlorohydrates (see J. Soc. Cosm. Chem. 24, 281 (1973)). Under the trade mark Locron® of Hoechst AG, Frankfurt (FRG), there is available commercially, for example, an aluminium chlorohydrate corresponding to formula Al₂(OH)₅Cl×2.5H₂O, the use of which is especially preferred (see J. Pharm. Pharmacol. 26, 531 (1975)). Besides the chlorohydrates, it is also possible to use aluminium hydroxyacetates and acidic aluminium/zirconium salts. Esterase inhibitors may be added as further deodorising active ingredients. Such inhibitors are preferably trialkyl citrates, such as trimethyl citrate, tripropyl citrate, triisopropyl citrate, tributyl citrate and especially triethyl citrate (Hydagen CAT, Henkel), which inhibit enzyme activity and hence reduce odour formation. Further substances that come into consideration as esterase inhibitors are sterol sulfates or phosphates, for example lanosterol, cholesterol, campesterol, stigmasterol and sitosterol sulfate or phosphate, dicarboxylic acids and esters thereof, for example glutaric acid, glutaric acid monoethyl ester, glutaric acid diethyl ester, adipic acid, adipic acid monoethyl ester, adipic acid diethyl ester, malonic acid and malonic acid diethyl ester and hydroxycarboxylic acids and esters thereof, for example citric acid, malic acid, tartaric acid or tartaric acid diethyl ester. Antibacterial active ingredients that influence the germ flora and kill or inhibit the growth of sweat-decomposing bacteria can likewise be present in the preparations (especially in stick preparations). Examples include chitosan, phenoxyethanol and chlorhexidine gluconate. 5-chloro-2-(2,4-dichlorophenoxy)-phenol (Triclosan, Irgasan, Ciba Specialty Chemicals Inc.) has also proved especially effective.

Anti-Dandruff Agents

As anti-dandruff agents there may be used, for example, climbazole, octopirox and zinc pyrithione. Customary film formers include, for example, chitosan, microcrystalline chitosan, quaternised chitosan, polyvinylpyrrolidone, vinylpyrrolidone/vinyl acetate copolymers, polymers of quaternary cellulose derivatives containing a high proportion of acrylic acid, collagen, hyaluronic acid and salts thereof and similar compounds.

Antioxidants

In addition to the primary light-protective substances it is also possible to use secondary light-protective substances of the antioxidant kind that interrupt the photochemical reaction chain triggered when UV radiation penetrates the skin or hair. Typical examples of such anti-oxidants are amino acids (e.g. glycine, histidine, tyrosine, tryptophan) and derivatives thereof, imidazoles (e.g. urocanic acid) and derivatives thereof, peptides, such as D,L-carnosine, D-carnosine, L-carnosine and derivatives thereof (e.g. anserine), carotinoids, carotenes, lycopene and derivatives thereof, chlorogenic acid and derivatives thereof, lipoic acid and derivatives thereof (e.g. dihydrolipoic acid), aurothioglycose, propylthiouracil and other thiols (e.g. thioredoxin, glutathione, cysteine, cystine, cystamine and the glycosyl, N-acetyl, methyl, ethyl, propyl, amyl, butyl, lauryl, palmitoyl, oleyl, linoleyl, cholesteryl and glyceryl esters thereof) and also salts thereof, dilauryl thiodipropionate, distearyl thiodipropionate, thiodipropionic acid and derivatives thereof (esters, ethers, peptides, lipids, nucleotides, nucleosides and salts) and also sulfoximine compounds (e.g. buthionine sulfoximines, homocysteine sulfoximine, buthionine sulfones, penta-, hexa-, hepta-thionine sulfoximine), also (metal) chelating agents (e.g. hydroxy fatty acids, palmitic acid phytic acid, lactoferrin), hydroxy acids (e.g. citric acid, lactic acid, malic acid), humic acid, bile acid, bile extracts, bilirubin, biliverdin, EDTA, EDDS, EGTA and derivatives thereof, unsaturated fatty acids and derivatives thereof (e.g. linolenic acid, linoleic acid, oleic acid), folic acid and derivatives thereof, ubiquinone and ubiquinol and derivatives thereof, vitamin C and derivatives (e.g. ascorbyl palmitate, magnesium ascorbyl phosphate, ascorbyl acetate), tocopherols and derivatives (e.g. vitamin E acetate), vitamin A and derivatives (e.g. vitamin A palmitate) and also coniferyl benzoate of benzoin resin, rutinic acid and derivatives thereof, glycosylrutin, ferulic acid, furfurylidene glucitol, carnosine, butyl hydroxytoluene, butyl hydroxyanisole, nordihydroguaiaretic acid, trihydroxybutyrophenone, uric acid and derivatives thereof, mannose and derivatives thereof, superoxide dismutase, N-[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionyl]sulfanilic acid (and salts thereof, for example the disodium salts), zinc and derivatives thereof (e.g. ZnO, ZnSO₄), selenium and derivatives thereof (e.g. selenium methionine), stilbene and derivatives thereof (e.g. stilbene oxide, trans-stilbene oxide) and the derivatives suitable according to the invention (salts, esters, ethers, sugars, nucleotides, nucleosides, peptides and lipids) of those mentioned active ingredients. HALS (=“Hindered Amine Light Stabilizers”) compounds may also be mentioned. The amount of antioxidants present is usually from 0.001 to 30% by weight, preferably from 0.01 to 3% by weight, based on the weight of the UV absorber of formula (1).

Hydrotropic Agents

To improve the flow behaviour it is also possible to employ hydrotropic agents, for example ethoxylated or non ethoxylated mono-alcohols, diols or polyols with a low number of carbon atoms or their ethers (e.g. ethanol, isopropanol, 1,2-dipropanediol, propyleneglycol, glyerin, ethylene glycol, ethylene glycol monoethylether, ethylene glycol monobutylether, propylene glycol monomethylether, propylene glycol monoethylether, propylene glycol monobutylether, diethylene glycol monomethylether; diethylene glycol monoethylether, diethylene glycol monobutylether and similar products). The polyols that come into consideration for that purpose have preferably from 2 to 15 carbon atoms and at least two hydroxy groups. The polyols may also contain further functional groups, especially amino groups, and/or may be modified with nitrogen. Typical examples are as follows: glycerol, alkylene glycols, for example ethylene glycol, diethylene glycol, propylene glycol, butylene glycol, hexylene glycol and also polyethylene glycols having an average molecular weight of from 100 to 1000 Dalton; technical oligoglycerol mixtures having an intrinsic degree of condensation of from 1.5 to 10, for example technical diglycerol mixtures having a diglycerol content of from 40 to 50% by weight; methylol compounds, such as, especially, trimethylolethane, trimethylolpropane, trimethylolbutane, pentaerythritol and dipentaerythritol; lower alkyl-glucosides, especially those having from 1 to 8 carbon atoms in the alkyl radical, for example methyl and butyl glucoside; sugar alcohols having from 5 to 12 carbon atoms, for example sorbitol or mannitol; sugars having from 5 to 12 carbon atoms, for example glucose or saccharose; amino sugars, for example glucamine; dialcohol amines, such as diethanolamine or 2-amino-1,3-propanediol.

Preservatives and Bacteria-Inhibiting Agents

Suitable preservatives include, for example, Methyl-, Ethyl-, Propyl-, Butyl-parabens, Benzalkonium chloride, 2-Bromo-2-nitro-propane-1,3-diol, Dehydroacetic acid, Diazolidinyl Urea, 2-Dichloro-benzyl alcohol, DMDM hydantoin, Formaldehyde solution, Methyldibromoglutanitrile, Phenoxyethanol, Sodium Hydroxymethylglycinate, Imidazolidinyl Urea, Triclosan and further substance classes listed in the following reference: K. F. DePolo—A short textbook of cosmetology, Chapter 7, Table 7-2, 7-3, 7-4 and 7-5, p 210-219.

Bacteria-Inhibiting Agents

Typical examples of bacteria-inhibiting agents are preservatives that have a specific action against gram-positive bacteria, such as 2,4,4′-trichloro-2′-hydroxydiphenyl ether, chlorhexidine (1,6-di(4-chlorophenyl-biguanido)hexane) or TCC (3,4,4′-trichlorocarbanilide). A large number of aromatic substances and ethereal oils also have antimicrobial properties. Typical examples are the active ingredients eugenol, menthol and thymol in clove oil, mint oil and thyme oil. A natural deodorising agent of interest is the terpene alcohol farnesol (3,7,11-trimethyl-2,6,10-dodecatrien-1-ol), which is present in lime blossom oil. Glycerol monolaurate has also proved to be a bacteriostatic agent. The amount of the additional bacteria-inhibiting agents present is usually from 0.1 to 2% by weight, based on the solids content of the preparations.

Perfume Oils

There may be mentioned as perfume oils mixtures of natural and/or synthetic aromatic substances. Natural aromatic substances are, for example, extracts from blossom (lilies, lavender, roses, jasmine, neroli, ylang-ylang), from stems and leaves (geranium, patchouli, petitgrain), from fruit (aniseed, coriander, carraway, juniper), from fruit peel (bergamot, lemons, oranges), from roots (mace, angelica, celery, cardamom, costus, iris, calmus), from wood (pinewood, sandalwood, guaiacum wood, cedarwood, rosewood), from herbs and grasses (tarragon, lemon grass, sage, thyme), from needles and twigs (spruce, pine, Scots pine, mountain pine), from resins and balsams (galbanum, elemi, benzoin, myrrh, olibanum, opoponax). Animal raw materials also come into consideration, for example civet and castoreum. Typical synthetic aromatic substances are, for example, products of the ester, ether, aldehyde, ketone, alcohol or hydrocarbon type. Aromatic substance compounds of the ester type are, for example, benzyl acetate, phenoxyethyl isobutyrate, p-tert-butylcyclohexyl acetate, linalyl acetate, dimethylbenzylcarbinyl acetate, phenylethyl acetate, linalyl benzoate, benzyl formate, ethylmethylphenyl glycinate, allylcyclohexyl propionate, styrallyl propionate and benzyl salicylate. The ethers include, for example, benzyl ethyl ether; the aldehydes include, for example, the linear alkanals having from 8 to 18 hydrocarbon atoms, citral, citronellal, citronellyl oxyacetaldehyde, cyclamen aldehyde, hydroxycitronellal, lilial and bourgeonal; the ketones include, for example, the ionones, isomethylionone and methyl cedryl ketone; the alcohols include, for example, anethol, citronellol, eugenol, isoeugenol, geraniol, linalool, phenyl ethyl alcohol and terpinol; and the hydrocarbons include mainly the terpenes and balsams. It is preferable, however, to use mixtures of various aromatic substances that together produce an attractive scent. Ethereal oils of relatively low volatility, which are chiefly used as aroma components, are also suitable as perfume oils, e.g. sage oil, camomile oil, clove oil, melissa oil, oil of cinnamon leaves, lime blossom oil, juniper berry oil, vetiver oil, olibanum oil, galbanum oil, labolanum oil and lavandin oil. Preference is given to the use of bergamot oil, dihydromyrcenol, lilial, lyral, citronellol, phenyl ethyl alcohol, hexyl cinnamaldehyde, geraniol, benzyl acetone, cyclamen aldehyde, linalool, boisambrene forte, ambroxan, indole, hedione, sandelice, lemon oil, tangerine oil, orange oil, allyl amyl glycolate, cyclovertal, lavandin oil, muscatel sage oil, damascone, bourbon geranium oil, cyclohexyl salicylate, vertofix coeur, iso-E-Super, Fixolide NP, evemyl, iraldein gamma, phenylacetic acid, geranyl acetate, benzyl acetate, rose oxide, romillat, irotyl and floramat alone or in admixture with one another.

Colourants

There may be used as colourants the substances that are suitable and permitted for cosmetic purposes, as compiled, for example, in the publication “Kosmetische Färbemittel” of the Farbstoffkommission der Deutschen Forschungsgemeinschaft, Verlag Chemie, Weinheim, 1984, pages 81 to 106. The colourants are usually used in concentrations of from 0.001 to 0.1% by weight, based on the total mixture.

Other Adjuvants

It is furthermore possible for the cosmetic preparations to contain, as adjuvants, anti-foams, such as silicones, structurants, such as maleic acid, solubilisers, such as ethylene glycol, propylene glycol, glycerol or diethylene glycol, opacifiers, such as latex, styrene/PVP or styrene/acrylamide copolymers, complexing agents, such as EDTA, NTA, alaninediacetic acid or phosphonic acids, propellants, such as propane/butane mixtures, N₂O, dimethyl ether, CO₂, N₂ or air, so-called coupler and developer components as oxidation dye precursors, reducing agents, such as thioglycolic acid and derivatives thereof, thiolactic acid, cysteamine, thiomalic acid or mercaptoethanesulfonic acid, or oxidising agents, such as hydrogen peroxide, potassium bromate or sodium bromate.

Suitable insect repellents are, for example, N,N-diethyl-m-toluamide, 1,2-pentanediol or insect repellent 3535; suitable self-tanning agents are, for example, dihydroxyacetone and/or erythrulose or dihydroxy acetone and/or dihydroxy acetone precursors as described in WO 01/85124 and/or erythrulose.

Polymeric Beads or Hollow Spheres as SPF Enhancers

The combination of the UV-absorbers and UV-absorber combinations, listed above, with SPF enhancers, such as non-active ingredients like Styrene/acrylates copolymer, silica beads, spheroidal magnesium silicate, crosslinked Polymethylmethacrylates (PMMA; Micopearl M305 Seppic), can maximize better the UV protection of the sun products. Holosphere additives (Sunspheres® ISP, Silica Shells hobo.) deflect radiation and the effective path length of the photon is therefore increased. (EP0893119). Some beads, as mentioned previously, provide a soft feel during spreading. Moreover, the optical activity of such beads, e.g. Micropearl M305, cans modulate skin shine by eliminating reflection phenomena and indirectly may scatter the UV light. When formulated in O/W emulsions, the preferably amount of such SPF enhancers should represent 1% to 10% of the total amount of the emulsion.

Cosmetic or Pharmaceutical Preparations

Cosmetic or pharmaceutical formulations are contained in a wide variety of cosmetic preparations. There come into consideration, for example, especially the following preparations:

-   -   skin-care preparations, e.g. skin-washing and cleansing         preparations in the form of tablet-form or liquid soaps,         soapless detergents or washing pastes,     -   bath preparations, e.g. liquid (foam baths, milks, shower         preparations) or solid bath preparations, e.g. bath cubes and         bath salts;     -   skin-care preparations, e.g. skin emulsions, multi-emulsions or         skin oils;     -   cosmetic personal care preparations, e.g. facial make-up in the         form of day creams or powder creams, face powder (loose or         pressed), rouge or cream make-up, eye-care preparations, e.g.         eyeshadow preparations, mascara, eyeliner, eye creams or eye-fix         creams; lip-care preparations, e.g. lipsticks, lip gloss, lip         contour pencils, nail-care preparations, such as nail varnish,         nail varnish removers, nail hardeners or cuticle removers;     -   foot-care preparations, e.g. foot baths, foot powders, foot         creams or foot balsams, special deodorants and antiperspirants         or callus-removing preparations;     -   light-protective preparations, such as sun milks, lotions,         creams or oils, sunblocks or tropicals, pre-tanning preparations         or after-sun preparations;     -   skin-tanning preparations, e.g. self-tanning creams;         depigmenting preparations, e.g. preparations for bleaching the         skin or skin-lightening preparations;     -   insect-repellents, e.g. insect-repellent oils, lotions, sprays         or sticks;     -   deodorants, such as deodorant sprays, pump-action sprays,         deodorant gels, sticks or roll-ons;     -   antiperspirants, e.g. antiperspirant sticks, creams or roll-ons;     -   preparations for cleansing and caring for blemished skin, e.g.         synthetic detergents (solid or liquid), peeling or scrub         preparations or peeling masks;     -   hair-removal preparations in chemical form (depilation), e.g.         hair-removing powders, liquid hair-removing preparations, cream-         or paste-form hair-removing preparations, hair-removing         preparations in gel form or aerosol foams;     -   shaving preparations, e.g. shaving soap, foaming shaving creams,         non-foaming shaving creams, foams and gels, preshave         preparations for dry shaving, aftershaves or aftershave lotions;     -   fragrance preparations, e.g. fragrances (eau de Cologne, eau de         toilette, eau de parfum, parfum de toilette, perfume), perfume         oils or perfume creams;     -   cosmetic hair-treatment preparations, e.g. hair-washing         preparations in the form of shampoos and conditioners, hair-care         preparations, e.g. pretreatment preparations, hair tonics,         styling creams, styling gels, pomades, hair rinses, treatment         packs, intensive hair treatments, hair-structuring preparations,         e.g. hair-waving preparations for permanent waves (hot wave,         mild wave, cold wave), hair-straightening preparations, liquid         hair-setting preparations, hair foams, hairsprays, bleaching         preparations, e.g. hydrogen peroxide solutions, lightening         shampoos, bleaching creams, bleaching powders, bleaching pastes         or oils, temporary, semi-permanent or permanent hair colourants,         preparations containing self-oxidising dyes, or natural hair         colourants, such as henna or camomile.         Presentation Forms

The final formulations listed may exist in a wide variety of presentation forms, for example:

-   -   in the form of liquid preparations as a W/O, O/W, O/W/O, W/O/W         or PIT emulsion and all kinds of microemulsions,     -   in the form of a gel,     -   in the form of an oil, a cream, milk or lotion,     -   in the form of a powder, a lacquer, a tablet or make-up,     -   in the form of a stick,     -   in the form of a spray (spray with propellent gas or pump-action         spray) or an aerosol,     -   in the form of a foam, or     -   in the form of a paste.

Of special importance as cosmetic preparations for the skin are light-protective preparations, such as sun milks, lotions, creams, oils, sunblocks or tropicals, pretanning preparations or after-sun preparations, also skin-tanning preparations, for example self-tanning creams. Of particular interest are sun protection creams, sun protection lotions, sun protection milk and sun protection preparations in the form of a spray.

Of special importance as cosmetic preparations for the hair are the above-mentioned preparations for hair treatment, especially hair-washing preparations in the form of shampoos, hair conditioners, hair-care preparations, e.g. pretreatment preparations, hair tonics, styling creams, styling gels, pomades, hair rinses, treatment packs, intensive hair treatments, hair-straightening preparations, liquid hair-setting preparations, hair foams and hairsprays. Of special interest are hair-washing preparations in the form of shampoos.

A shampoo has, for example, the following composition: from 0.01 to 5% by weight of a UV absorber according to the invention, 12.0% by weight of sodium laureth-2-sulfate, 4.0% by weight of cocamidopropyl betaine, 3.0% by weight of sodium chloride, and water ad 100%.

For example, especially the following hair-cosmetic formulations may be used:

-   a₁) spontaneously emulsifying stock formulation, consisting of the     UV absorber according to the invention, PEG-6-C₁₀oxoalcohol and     sorbitan sesquioleate, to which water and any desired quaternary     ammonium compound, for example 4% minkamidopropyl     dimethyl-2-hydroxyethylammonium chloride or Quaternium 80 is added; -   a₂) spontaneously emulsifying stock formulation consisting of the UV     absorber according to the invention, tributyl citrate and     PEG-20-sorbitan monooleate, to which water and any desired     quaternary ammonium compound, for example 4% minkamidopropyl     dimethyl-2-hydroxyethylammonium chloride or Quaternium 80 is added; -   b) quat-doped solutions of the UV absorber according to the     invention in butyl triglycol and tributyl citrate; -   c) mixtures or solutions of the UV absorber according to the     invention with n-alkylpyrrolidone.

Other typical ingredients in such formulations are preservatives, bactericides and bacteriostatic agents, perfumes, dyes, pigments, thickening agents, moisturizing agents, humectants, fats, oils, waxes or other typical ingredients of cosmetic and personal care formulations such as alcohols, poly-alcohols, polymers, electrolytes, organic solvents, silicon derivatives, emollients, emulgators or emulsifying surfactants, surfactants, dispersing agents, antioxidants, anti-irritants and anti-inflammatory agents etc.

Examples of Cosmetic and Pharmaceutical Preparations (X=Preferred Combinations)

O/W systems: Ingredients Emulsifiers 1 2 3 4 5 6 7 8 Potassium Cetyl Phosphate 2%-5% X Cetearyl Alcohol/Dicetyl Phosphate/ X Ceteth-10 Phosphate 2%-6% Sodium Stearyl Phtalamate 1%-2% X Cetearyl Alcohol/Behentrimonium X Methosulfate 1%-5% Quaternium-32 1%-5% X Dimethicone copolyol/Caprylic/Capric X Triglyceride 1%-4% Steareth-2/Steareth-21 2%-5% X Polyglyceryl Methyl Glucose X Distearate 1%-4% Lipophilic emollient/dispersant X X X X X X X X oil 15%-20% Fatty Alcohols and/or Waxes 1%-5% X X X X X X X X Thickeners (water swellable X X X X X X X X thickeners) 0.5%-1.5% Preservatives 0.5%-1% X X X X X X X X Chelating agents (such as EDTA) X X X X X X X X 0%-0.2% Antioxidants 0.05%-0.2% X X X X X X X X Water deionized Qs 100% X X X X X X X X Perfume oils 0.1%-0.4% X X X X X X X X UV-absorber according to the X X X X X X X X invention 1%-20% UV-absorber as described in X X X X X X X X table 1-3 0%-30%

W/O systems Ingredients Emulsifiers 1 2 3 4 5 Polyglyceryl-2 Dipolyhydroxystearate 2%-4% X PEG-30 Dipolyhydroxystearate 2%-4% X Rapeseed Oil Sorbitol Esters 1%-5% X PEG-45/Dodecyl Glycol Copolymer 1%-5% X Sorbitan Oleate/Polycerol-3 ricinoleate 1%-5% X Lipophilic emollient/dispersant oil 10%-20% X X X X X Fatty Alcohols and/or Waxes 10%-15% X X X X X Electrolytes (NaCl, MgSO₄) 0.5%-1% X X X X X Polyol phase (Propylene glycol, glycerin) 1%-8% X X X X X Preservaties 0.3%-0.8% X X X X X Perfume oils 0.1%-0.4% X X X X X Chelating agents (such as EDTA) 0%-0.2% X X X X X Antioxidants 0.05%-0.2% X X X X X Water deionized Qs 100% X X X X X UV-absorber according to the invention 1%-20%. X X X X X UV-absorber as described in table 1-3 0%-30%. X X X X X

W/Silicone systems Ingredients 1 2 3 4 Emulsifiers Dimethicone Copolyol/Cyclomethicone 5%-10% X X Laurylmethicone Copolyol 5%-10% X X Silicone phase Cyclopentasiloxane 15%-25% X X Dimethicone 15%-25% X X Silicone elastomer Dimethicone/Vinyldimethicone Crosspolymer X X X X 1%-10% Humectant/polyols (Propylene glycol, glycerin . . .) X X X X 2%-8% Chelating agents (such as EDTA) 0%-0.2% X X X X Antioxidants 0.05%-0.2% X X X X Preservatives 0.3%-0.8% X X X X Perfume oils 0.1%-0.4% X X X X Water deionized Qs 100% X X X X UV-absorber according to the invention 1%-20% X X X X UV-absorber as described in table 1-3 0%-30% X X X X

Multiple emulsions Ingredients 1 2 3 4 5 6 7 8 9 10 11 12 Primary emulsion W1/O PEG-30 Dipolyhydroxystearate X X X 2%-6% Cetyl Dimethicone Copolyol X X 1%-3% PEG-30 Dipolyhydroxystearate/ X X Steareth-2/Steareth-21 4%-6% Polyglyceryl-2 Dipolyhydroxystearate X X 1%-3% Polyglyceryl-6 Ricinoleate 1%-3% X X X Oil phase 15%-30% Fatty acid esters X X X X X X X Natural and synthetic Triglycerides X X X X X X X Hydrocarbon oils X X X X X X X Silicone oils X X X X X X X Preservatives 0.3%-0.8% X X X X X X X X X X X X Water Deioniz. qs 100% X X X X X X X X X X X X Ionic monofunctional O/W emulsifiers Sorbitan Stearate/Sucrose Cocoate X X X 3%-7% Sucrose Laurate 3%-7% X X X Poloxamer 407 3%-7% X X X Polyoxyethylene(20)Sorbate X X X Monoleate 3%-5% Primary emulsion W1/O 50% X X X X X X X X X X X X Thickeners (water swellable X X X X X X X X X X X X polymers) 0.3%-1% Water deionized Qs 100% X X X X X X X X X X X X Perfume oils 0.1%-0.4% X X X X X X X X X X X X UV-absorber according to the X X X X X X X X X X X X invention 1%-20% UV-absorber as described in table X X X X X X X X X X X X 1-3 0%-30%

O1/W/O2 emulsions Ingredients Primary emulsion O1/W 1 2 3 4 5 6 7 8 PEG-60 Hydrogenated X X X X Castor Oil 25% Steareth-25 25% X X X X Oil phase 75% Fatty acid esters X X Natural and synthetic Triglycerides X X Hydrocarbon oils X X Silicone oils X X Preservatives 0.3%-0.8% X X X X X X X X Water deionized Qs 100% X X X X X X X X Non ionic multifunctional X X X X X X X X W/O emulsifier 2%-5% Waxes 1%-5% X X X X X X X X Oil phase 20%-30% X X X X X X X X Fatty acid esters Natural and synthetic Triglycerides Hydrocarbon oils Silicone oils Primary emulsion O1/W 15% X X X X X X X X Electrolytes (NaCl, X X X X X X X X MgSO₄) 0.1%-0.5% Water deionized Qs 100% X X X X X X X X Perfume oils 0.1%-0.4% X X X X X X X X UV-absorber according to X X X X X X X X the invention 1%-20% UV-absorber as described X X X X X X X X in table 1-3 0%-30%

Microemulsions Ingredients 1 2 3 4 5 6 7 8 9 10 Surfactants PEG-8 Caprylic/Capric X X X X X Glycerides 10%-25% PPG-5-ceteth-20 X X X X X 10%-25% Co-surfactants Polyglyceryl-6 Isostearate X X 5%-15% Polyglyceryl-3 X X Diisostearate 5%-15% Polyglyceryl-6 Dioleate X X 5%-15% PPG-10 Cetyl Ether X X 5%-15% Ethoxydiglycol 5%-15% X X Oil phase 10%-80% X X X X X X X X X X Isostearyl Benzoate Isostearyl Isostearate PEG-7 Glyceryl Cocoate Cyclomethicone Polyalcohols/Humectants X X X X X X X X X X 1%-10% Preservatives 0.3-0.8% X X X X X X X X X X Perfume oils 0.1%-0.4% X X X X X X X X X X Water Deioniz. qs 100% X X X X X X X X X X UV-absorber according to X X X X X X X X X X the invention 1%-20% UV-absorber as described X X X X X X X X X X in table 1-3 0%-30%

O/W Spray emulsions Ingredients 1 2 3 4 5 6 Emulsifiers Alkyl Phosphates 0.1%-5% X X X Glucosidic derivatives 0.1%-5% X X X Solubilisants Ethoxylated Glyceryl ethers 0.1%-1% X X Polysorbates 0.1%-1% X X Ethoxylated Oleyl ethers 0.1%-1% X X Film forming agents PVP/VA Coplymer 1%-10% X X X PVM/MA Copolymer 1%-10% X X X Oil phase 5%-20% X X X X X X Natural oils(Meadowfoam, Jojoba, Macadamia . . .) Fatty acids esters Mineral oils Silicone oils Alcohol 0%-50% X X X X X X Thickeners 0.1%-0.5% X X X X X X Polyacrylates Aluminium/Magnesium Silicates Gums Neutralizing agents 0%-1% X X X X X X Polyalcohols/Humectants 1%-5% X X X X X X Chelating agents (such as EDTA) 0%-0.2% X X X X X X Antioxidants 0.05%-0.2% X X X X X X Water Deioniz. qs 100% X X X X X X Perfume oils 0.1%-0.5% X X X X X X Preservatives 0.4%-1% X X X X X X UV-absorber according to the X X X X X X invention 1%-20% UV-absorber as described X X X X X X in table 1-3 0%-30%

G - Aqueous Ingredients 1 2 3 4 5 6 7 8 9 10 11 12 Thickeners Natural Thickener 1%-5% X X X X Semi-symthetic Thickener 1%-5% X X X X Synthetic Thickener 0.3%-1.3% X X X X Neutralizing Agents 0.5%-1.5% X X X X X X X X X X X X Polyols - Humectants 5%-50% X X X X X X X X X X X X Film forming agent/Conditioner Polyquaternium series 1%-5% X X X X X X PVM/MA Copolymer 1%-5% X X X X X X Preservatives 0.5%-1% X X X X X X X X X X X X Chelating Agents (as EDTA) X X X X X X X X X X X X <0.1% Water Deioniz. qs 100% X X X X X X X X X X X X Perfume oils 0.05%-0.4% X X X X X X X X X X X X Solubilisants Ethoxylated Glyceryl ethers X X X 0.1%-5% Polysorbates 0.1%-5% X X X Ethoxylated Oleyl ethers X X X X X X 0.1%-5% UV-absorber according to the X X X X X X X X X X X X invention 1%-20% UV-absorber as described in table X X X X X X X X X X X X 1-3 0%-30%

Oleogels Ingredients 1 2 3 4 5 6 7 8 9 10 Thickeners Hydrogenated Lecithin 1%-10% X X Silica Dimethyl Silylate 1%-10% X X Silica 1%-5% X X C₂₄₋₂₈ Alkyl Dimethicone 1%-5% X X Aluminium or Magnesium Stearate 1%-5% X X Polyols - Humectants 5%-70% X X X X X X X X X X Oil phase 20%-90% Dicaprylyl Ether X X X Phenyl Trimethicone X X Hydrogenated Polyisobutene X Isopropyl Isostearate X X Oleogel basis (Mineral oil and hydrogenated X X Butylene/Ethylene or Ethylene/Propylene Styrene Copolymer) Silicone wax 1%-10% X X X X X X X X X X Dimethiconol Behenate Dimethiconol Stearate Perfume oils 0.1%-0.5% X X X X X X X X X X Antioxidants 0.05%-0.2% X X X X X X X X X X UV-absorber according to the invention X X X X X X X X X X 1%-20% UV-absorber as described in table 1-3 X X X X X X X X X X 0%-30%

Light/dry cosmetic oils Ingredients 1 2 3 4 Lipophilic base Hydrocarbon oils 30%-70% X X Fatty acid esters branched or not 10%-50% X X Light feel agent Silicones/Siloxanes 0%-10% X X Perfluorinated oils and Perfluoroethers 0%-10% X X Viscosifying agents 0%-10% X X X X Waxes Esters of long chain acids and alcohols 0%-2% X X X X Antioxidants 0.1%-1% X X X X Solubilisants/dispersing agents 0%-5% X X X X Perfume oils 0.1%-0.5% X X X X UV-absorber according to the invention 1%-20%. X X X X UV-absorber as described in table 1-3 0%-30% X X X X

Foaming/mousse products Ingredients SD Alcohol 40 0%-8% X Propellant 8%-15% X Nonionic Emulsifier/Surfactant 0.5%-3% X Corrosion Inhibitor 0%-1% X Perfume oils 0.1%-0.5% X Preservatives 0.1%-1% X Miscellaneous 0%-1% X UV-absorber according to the invention 1%-20%. X UV-absorber as described in table 1-3 0%-30% X

Stick products Ingredients Waxes 15%-30% X Natural and silicone oils 20%-75% X Lanoline derivatives 5%->50% X Esters of lanolin x Acetylated lanolin x Lanolin oil x Colorants and pigments 10%-15% X Antioxidants 0.1%-0.8% X Perfume oils 0.1%-2% X Preservatives 0.1%-0.7% X UV-absorber according to the invention 1%-20% X UV-absorber as described in table 1-3 0%-30% X

Liquid and compact Ingredients 1 2 Liquid foundation Powder phase 10%-15% X Oil phase 30%-40%; 75% (only for anhydrous form) X Thickener/suspending agents 1%-5% X Film forming polymers 1%-2% X Antioxidants 0.1%-1% X Perfume oils 0.1%-0.5% X Preservatives 0.1%-0.8% X Water deionized Qs 100% X Compact powder Powder phase 15%-50% X Oil phase 15%-50% X Polyol phase 5%-15% X Antioxidants 0.1%-1% X Perfume oils 0.1%-0.5% X Preservatives 0.1%-0.8% X For the two product forms UV-absorber according to the invention 1%-20% X X UV-absorber as described in table 1-3 0%-30% X X

Conditioning Shampoos Ingredients 1 Primary surfactants (listed previously) 5%-10% X Secondary surfactants (listed previously) 5%-15% X Foam Stabilizers (listed previously) 0%-5% X Water deionized 40%-70% X Actives 0-10% X Conditioners x Refatting agents x Moisturizing agents x Thickeners/Rheology mofifiers 0%-3% X Humectants 0%-2% X PH adjusting agents 0%-1% X Preservatives 0.05%-1% X Perfume oils 0.1%-1% X Antioxidants 0.05%-0.20% X Chelating Agents (EDTA) 0%-0.2% X Opascifying agents 0%-2% X UV-absorber according to the invention 1%-20% X UV-absorber as described in table 1-3 0%-30% X

The cosmetic preparation according to the invention is distinguished by excellent protection of human skin against the damaging effect of sunlight.

In the following Examples percentages relate to weight and the temperature is given in ° Celsius.

EXAMPLES Example 1 Preparation of the Compound of Formula

A mixture consisting of 6.4 g 4-aminobenzoeacidethylester (0.025 mol), 8.7 g N,N-dimethylacetamid (0.0527) and 20 ml dioxan (0.23 mol) are added drop by drop to a solution of 6.4 g 2,4-dichloro-6-(4-methoxyphenyl)-[1,3,5]-triazine (0.025 mol) in 80 ml dioxan (0.92). The reaction solution is stirred 4.5 h at 80° C. Afterwards 100 ml water (0.18 mol) is added slowly.

The reaction product is filtered off at 20° C. and washed with dioxan and water. The reaction is also recrystallized with dimethylformamide boiled in methanol.

The obtained product is dried in vacuum. The yield of the white product is 4.2 g (32.7%).

Example 2

Analogous to Example 1 the compound of formula (102)

is obtained if, 4-aminobenzoic-(2-ethyl-hexyl)ester is used instead of 4-aminobenzoic acid ethylester.

Example 3

Analogous to Example 1 the compound of formula

is obtained, if 4-aminobenzoic acid methylester is used instead of 4-aminobenzoic acid ethylester.

Example 4

Analogous to Example 1 the compound of formula

is obtained if 4-aminobenzoic acid is used instead of 4-aminobenzoic acid ethylester.

Example 5

Analogous to Example 1 the compound of formula

is obtained if 4-amino benzoic acidamide is used instead of 4-aminobenzoic acid ethylester.

Example 6

100 parts of the compound of formula

are grounded together with grounding aids for example consisting of zirkonium silicate (balls diameter: 0.1 to 4 mm), a dispersing agent (15 parts of alkyl polyglucoside) and water (85 parts) in a ball mill until a micropigment is obtained with an average particle size of d₅₀=200 nm.

A mikropigment-dispersion of the corresponding UV absorber is so obtained.

APPLICATION EXAMPLES Example 7 UV-A/UV-B Daily Care UV Protection Lotion

Composition % w/w INCI-Name (as supplied) Part A Oleth-3 Phosphate 0.60 Steareth-21 2.50 Steareth-2 1.00 Cetyl Alcohol 0.80 Stearyl Alcohol 1.50 Tribehenin 0.80 Isohexadecane 8.00 Ethylhexyl Methoxycinnamate 5.00 Part B Water qs to 100 Glycerin 2.00 UV-absorber dispersion as prepared in example 6 3.00 Disodium EDTA 0.10 Part C Water 20.00 Diazolidinyl Urea (and) Iodopropynyl 0.15 Butylcarbamate Propylene Glycol 4.00 Part D Sodium Acrylates Copolymer (and) 1.50 Paraffinium Liquidum (and) PPG-1 Trideceth-6 Cyclopentasiloxane 4.50 PEG-12 Dimethicone 2.00 Tocopheryl Acetate 0.45 Water (and) Citric Acid qs Part E Fragrance qs Preparation

Part A and part B are heated separately to 75° C. Part A is poured into part B under continuous stirring. Immediately after the emulsification Cyclopentasiloxane and PEG-12 Dimethicone from part D are incorporated in the mixture. Afterwards the mixture is homogenized with an Ultra Turrax at 11 000 rpm for 30 sec. and is cooled down to 65° C. and Sodium Acrylates Copolymer (and) Paraffinium Liquidum (and) PPG-1 Trideceth-6 is incorporated. Part C is added at a temperature <50° C. At 35° C. or below Tocopheryl Acetate is incorporated and subsequently the pH is adjusted with Citric Acid Solution. Part E is added at room temperature.

Example 8 UV Day Lotion

Composition % w/w INCI-Name (as supplied) Part A Cetyl Phosphate 1.75 C₁₂-C₁₅ Alkyl Benzoate 5.00 Cetearyl Alcohol/PEG-20 Stearate 2.00 Ethoxydiglycol Oleate 2.00 Stearic Acid 1.50 Ethylhexyl Methoxycinnamate 3.00 Isononyl Isononanoate 2.00 Part B Aqua qs to 100 Xanthan Gum 0.35 UV-absorber dispersion as prepared in example 6 5.00 Disodium EDTA 0.20 Propylene Glycol 2.00 Diazolidinyl Urea (and) Methylparaben (and) 0.70 Propylparaben (and) Propylene Glycol Glycerin 1.50 Part C Cyclopentasiloxane (and) Dimethiconol 1.00 Ethoxydiglycol 3.00 Dimethicone 2.00 Part D Triethanolamine qs Preparation

Part A is prepared by incorporating all ingredients, then stirred under moderate speed and heated to 75° C. Part B is prepared and heated to 75° C. At this temperature part B is poured into part A under progressive stirring speed, then homogenized (30 sec., 15000 rpm). Below 55° C. the ingredients of part C are incorporated. After cooling down under moderate stirring the pH is checked and adjusted with triethanolamine.

Example 9 Sun Protection Emulsion

Composition % w/w INCI-Name (as supplied) Part A Cetearyl Alcohol (and) Dicetyl Phosphate (and) 4.00 Ceteth-10 Phosphate C12-15 Alkyl Benzoate 2.00 Dicaprylyl Ether 3.00 Ethoxydiglycol Oleate 2.00 Stearic Acid 1.00 Ethylhexyl Methoxycinnamate 3.00 Sodium Acrylates Copolymer (and) Glycine Soja 0.30 (and) PPG-1 Trideceth-6 Squalane 3.50 Part B Aqua qs to 100 UV-absorber dispersion as prepared in example 6 5.00 Part C Diazolidinyl Urea (and) Iodopropynyl 0.15 Butylcarbamate Propylene Glycol 2.50 Aqua 10.00  Part D Cyclopentasiloxane, Dimethiconol 2.00 Ethoxydiglycol 5.00 Cyclopentasiloxane (and) Dimethicone/Vinyl- 2.00 dimethicone Crosspolymer Part E Sodium Hydroxide 0.10 Preparation

Part A is prepared by incorporating all ingredients, then stirred under moderate speed and heated to 75° C. Part B is prepared and heated to 75° C. At this temperature, part B is poured into part A under progressive stirring speed. Below 65° C., the ingredients of part D are added separately. After cooling down under moderate stirring to 55° C. part C is added. Then the pH is checked and adjusted with sodium hydroxide. The formulation is homogenized for 30 sec at 16000 rpm.

Example 10 Every Day Lotion

Composition % w/w INCI-Name (as supplied) Part A Stearyl Phosphate 5.00 Tricontanyl PVP 1.00 Ethoxydiglycol Oleate 3.00 Squalane 5.00 C₁₂₋₁₅ Alkyl Benzoate 5.00 Ethylhexyl Methoxycinnamate 3.00 Glyceryl Stearate 2.00 Cetyl Alcohol 2.00 Part B Aqua 20.00  UV-absorber dispersion as prepared in example 6 3.00 Part C Aqua qs to 100 Steareth-10 Allyl Ether/Acrylates Copolymer 0.50 Glycerin 2.50 Diazolidinyl Urea (and) Iodopropynyl 0.15 Butylcarbamate Sodium Lauroyl Glutamate 0.70 Part D Cyclopentasiloxane (and) Dimethiconol 1.50 Triethanolamine 1.85 Preparation

Part A is prepared by incorporating all ingredients, then stirred under moderate speed and heated to 75° C. Part C is prepared and heated to 75° C. Part C is poured into part A under moderate stirring. Immediately after the emulsification part B is added, then neutralized with a part of the triethanolamine. The formulation is homogenized for 30 sec. After cooling down under moderate stirring Cyclopentasiloxane (and) Dimethiconol are added. Below 35° C. the pH is checked and adjusted with triethanolamine.

Example 11 Sprayable Sunscreen Emulsion

Composition % w/w INCI-Name (as supplied) Part A Ceteareth-15 (and) Glyceryl Stearate 3.00 Stearyl Alcohol 1.00 Cetyl Ricinoleate 0.80 Dicaprylyl Ether 3.00 C₁₂₋₁₅ Alkyl Benzoate 3.00 Isohexadecane 2.50 Stearyl Dimethicone 1.00 Ethylhexyl Methoxycinnamate 4.00 Cetyl Alcohol 0.80 Di-C₁₂₋₁₃ Alkyl Tartrate 3.00 Part B Aqua qs to 100 Steareth-10 Allyl Ether/Acrylates Copolymer 0.45 PEG-7 Glyceryl Cocoate 2.50 Glycerin 2.00 Propylene Glycol 3.00 Part C Diazolidinyl Urea (and) Iodopropynyl 0.15 Butylcarbamate Aqua 20.00  UV-absorber dispersion as prepared in example 6 12.00  Titanium Dioxide (and) Silica (and) Sodium 8.00 Polyacrylate Part D Cyclopentasiloxane (and) Dimethiconol 0.85 Part E Sodium Hydroxide (and) Water qs to pH 6.50-7.00 Part F Fragrance qs Preparation

Part A and part B are heated up to 80° C. Part A is blended into part B under stirring and homogenized with an Ultra Turrax by 11 000 rpm for 30 sec. Part C is heated to 60° C. and added slowly to the emulsion. After cooling down to 40° C. part D is incorporated. Parts E and F are added at room temperature.

Example 12 Daily Care Lotion

Composition % w/w INCI-Name (as supplied) Part A Polyglyceryl Methyl Glucose Distearate 2.50 Cetearyl Alcohol 2.00 Octyl Stearate 3.00 Caprylic/Capric Triglyceride 4.00 Isohexadecane 4.00 Ethylhexyl Methoxycinnamate 2.70 Part B Aqua 64.80 Glycerin 5.00 Phenoxyethanol (and) Methylparaben (and) 0.50 Butylparaben (and) Ethylparaben (and) Propylparaben UV-absorber dispersion as prepared in example 6 8.00 Part C Cyclomethicone (and) Dimethicone 3.00 Part D Steareth-10 Allyl Ether/Acrylates Copolymer 0.50 Preparation

Part A and B are heated to 75° C. Part A is added into part B under continuous stirring and homogenized with 11000 rpm for one minute. After cooling down to 50° C. part C is added under continuous stirring. After cooling further down to 30° C. part D is added. Afterwards the pH is adjusted between 6.00-6.50.

Example 13 Daily Care with UV Protection

Composition % w/w INCI-Name (as supplied) Part A Glyceryl Stearate SE 3.00 Glyceryl Stearate and PEG-100 Stearate 3.50 Cetyl Alcohol 1.50 Myristyl Myristate 2.00 Isopropyl Palmitate 2.50 Paraffinum Perliquidum 5.00 Octyl Dimethyl PABA 3.00 Part B Aqua qs to 100 Propylene Glycol 7.50 Phenoxyethanol (and) Methylparaben (and) 1.00 Butylparaben (and) Ethylparaben (and) Propylparaben Part C Aqua 30.00 UV-absorber dispersion as prepared in example 6 10.00 Part D Sodium Acrylates Copolymer (and) Paraffinium 2.00 Liquidum (and) PPG-1 Trideceth-6 Part E Citric Acid 0.30 Preparation

Part A and B are heated separately to 75° C. After adding part B into part A the mixture is homogenized with Ultra Turrax for one minute at 11000 rpm. After cooling down to 50° C. part C is added. Afterwards the formulation is homogenized for one minute at 16000 rpm. Below 40° C. part D is added. At room temperature the pH-value is adjusted with part E between 6.00 and 6.50.

Example 14 O/W Every Day UV Protection Lotion

Composition % w/w INCI-Name (as supplied) Part A Glyceryl Stearate (and) PEG-100 Stearate 5.00 Stearyl Alcohol 1.00 Tripalmitin 0.70 Dimethicone 2.00 C₁₂₋₁₅ Alkyl Benzoate 5.00 Isopropyl Palmitate 5.00 Ethylhexyl Methoxycinnamate 3.00 Part B Water qs to 100 Polysorbate 60 0.50 Glycerin 3.00 Part C Water 10.00  UV-absorber dispersion as prepared in example 6 8.00 Part D Phenoxyethanol (and) Methylparaben (and) 0.70 Ethylparaben (and) Butylparaben (and) Propylparaben (and) Isobutylparaben Steareth-10 Allyl Ether/Acrylates Copolymer 1.50 Part E Water (and) Sodium Hydroxide qs Part F Fragrance qs Preparation

Part A and B are heated separately up to 75° C., part C to 60° C. Afterwards part B is poured into part A under stirring. The mixture is homogenized with an Ultra Turrax for 30 sec. at 11 000 rpm and part C is incorporated. After cooling down to 40° C. part D is added. At room temperature the pH-value is adjusted with sodium hydroxide between 6.30 and 6.70 and part F is added.

Example 15 O/W Every Day UV Protection

Composition % w/w INCI-Name (as supplied) Part A Glyceryl Stearate (and) PEG-100 Stearate 5.00 Stearyl Alcohol 1.00 Tripalmitin 0.70 Dimethicone 2.00 C₁₂₋₁₅ Alkyl Benzoate 5.00 Isopropyl Palmitate 5.00 Ethylhexyl Methoxycinnamate 3.00 Part B Water qs to 100 Polysorbate 60 0.50 Glycerin 3.00 Part C Water 10.00  UV-absorber dispersion as prepared in example 6 8.00 Part D Phenoxyethanol (and) Methylparaben (and) 0.70 Ethylparaben (and) Butylparaben (and) Propylparaben (and) Isobutylparaben Steareth-10 Allyl Ether/Acrylates Copolymer 1.50 Part E Water (and) Sodium Hydroxide qs Part F Fragrance qs Preparation

Part A and B are heated separately up to 75° C.; part C to 60° C. Afterwards part B is poured into part A under stirring. After homogenization with an Ultra Turrax for 30 sec. at 11 000 rpm part C is incorporated. After cooling down to 40° C. part D is added. At room temperature the pH-value is adjusted with sodium hydroxide between 6.30 and 6.70 and part F is added.

Example 16 Sunscreen Cream

Composition % w/w INCI-Name (as supplied) Part A Cetearyl Alcohol (and) Dicetyl Phosphate (and) 4.50 Ceteth-10 Phosphate C₁₂₋₁₅ Alkyl Benzoate 6.00 Caprylic/Capric Triglyceride 7.00 Pentaerythritol Tetraisostearate 2.00 Ethylhexyl Methoxycinnamate 3.00 Isoamyl p-Methoxycinnamate 2.00 Part B Aqua qs to 100 Glycerin 2.00 Propylene Glycol 1.50 Magnesium Aluminium Silicate 1.20 Part C Steareth-10 Allyl Ether/Acrylates Copolymer 0.50 UV-absorber dispersion as prepared in example 6 12.00  Part D Phenyl Trimethicone 1.50 Phenoxyethanol (and) Methylparaben (and) 0.70 Butylparaben (and) Ethylparaben (and) Propylparaben Part E sodium hydroxide 0.90 Preparation

Part A and part B are heated separately to 75° C. Part B is added into part A under continuous stirring and afterwards homogenized with Ultra Turrax for 30 sec at 11000 rpm. After cooling down to 60° C. part C is added. At 40° C. part C is added and homogenized for 15 sec at 11000 rpm. At room temperature the pH-value is adjusted with part E.

Example 17 UVA/UVB Daily Care Lotion, Type O/W

Composition % w/w INCI-Name (as supplied) Part A Glyceryl Stearate (and) PEG-100 Stearate 5.00 Stearyl Alcohol 1.00 Tripalmitin 0.70 Mineral Oil 15.00  Part B Water qs to 100 Polysorbate 60 0.50 Glycerin 3.00 Part C Water 10.00  UV-absorber dispersion as prepared in example 6 8.00 Part D Steareth-10 Allyl Ether/Acrylates Copolymer 1.50 Phenoxyethanol (and) Methylparaben (and) 0.70 Ethylparaben (and) Butylparaben (and) Propylparaben (and) Isobutylparaben Part E Water (and) Sodium Hydroxide qs Part F Fragrance qs Preparation

Part A and B are heated separately to 75° C.; part C to 60° C. Part B is poured into part A under stirring. After 1 minute the mixture is homogenized by 11000 rpm add part C is added to the mixture of A/B. After cooling down to 40° C. part D is incorporated. At room temperature the pH value is adjusted with part E between 6.3 and 7.0. Finally part F is added.

Example 18 UVA/UVB Daily Care Lotion, Type O/W

Composition % w/w INCI-Name (as supplied) Part A Oleth-3 Phosphate 0.60 Steareth-21 2.50 Steareth-2 1.00 Cetyl Alcohol 0.80 Stearyl Alcohol 1.50 Tribehenin 0.80 Isohexadecane 8.00 Part B Water qs to 100 Glycerin 2.00 Disodium EDTA 0.10 Part C Cyclopentasiloxane 4.50 PEG-12 Dimethicone 2.00 Part D Sodium Acrylates Copolymer 1.50 (and) Mineral Oil (and) PPG-1 Trideceth-6 Part E UV-absorber dispersion as prepared in example 6 10.00  Part F Tocopheryl Acetate 0.45 DMDM Hydantoin (and) Iodopropynyl 0.85 Butylcarbamate (and) Aqua (and) Butylene Glycol Part G Water (and) Citric Acid qs Fragrance qs Preparation

Part A and part B are heated separately to 75° C. Part A is poured into part B under stirring. Immediately after the emulsification, part C is added to the mixture and homogenized with an Ultra Turrax by 11000 rpm for 30 sec. After cooling down to 65° C. Sodium Acrylates Copolymer (and) Mineral Oil (and) PPG-1 Trideceth-6 is added. At 50° C. Part E is slowly added. At 35-30° C. part F is incorporated. The pH is adjusted with part G between 5.5 and 6.5.

Example 19 UV-A/UV-B Every Day Protection Lotion O/W

Composition % w/w INCI-Name (as supplied) Part A Glyceryl Dilaurate 2.00 Ethylhexyl Palmitate 6.00 Cetyl Alcohol 1.00 Glyceryl Stearate 2.00 Laureth-23 1.00 Isopropyl Palmitate 2.00 Tribehenin 0.80 Beeswax 1.50 Lanolin Oil 1.00 Part B Water qs to 100 Propylene Glycol 4.00 Water (and) Titanium Dioxide 4.00 (and) Alumina (and) Sodium Metaphosphate (and) Phenoxyethanol (and) Sodium Methylparaben Part C Steareth-10 Allyl Ether/Acrylates Copolymer 1.00 Part D Phenoxyethanol (and) Methylparaben 1.00 (and) Ethylparaben (and) Butylparaben (and) Propylparaben (and) Isobutylparaben UV-absorber dispersion as prepared in example 6 8.00 Part E Water (and) Sodium Hydroxide qs Preparation

Part A and part B are heated separately up to 80° C. Part A is poured into part B while stirring and homogenized with an Ultra Turrax by 11000 rpm for 30 sec. After cooling down to 60° C. part C is incorporated. At 40° C. part D is added slowly under continuous stirring. The pH is adjusted with part E between 6.50-7.00.

Example 20 Sprayable Sunscreen Lotion

Composition % w/w INCI-Name (as supplied) Part A Potassium Cetyl Phosphate 0.20 Isohexadecane 7.00 VP/Eicosene Copolymer 1.50 Di-C₁₂₋₁₃ Alkyl Tartrate 6.00 Ethylhexyl Triazone 2.50 C₁₂₋₁₅ Alkyl Benzoate 4.50 Part B Water qs to 100 Sorbeth-30 2.00 Sorbitan Stearate (and) Sucrose Cocoate 4.00 Titanium Dioxide (and) Alumina (and) 2.50 Silica (and) Sodium Polyacrylate Part C Water 30.00  UV-absorber dispersion as prepared in example 6 12.00  Part D Phenoxyethanol (and) Methylparaben 0.70 (and) Ethylparaben (and) Butylparaben (and) Propylparaben (and) Isobutylparaben Part E Water (and) Citric Acid qs Preparation

Part A and part B are heated separately up to 80° C., part C to 50° C. Part B is poured into part A and homogenized with an Ultra Turrax for 1 minute by 11000 rpm. After cooling down to 50° C. part C is added under continuous stirring. At 40° C. part D is incorporated and homogenized again for 10 sec. by 11000 rpm. The pH is adjusted with part E.

Example 21 O/W Every Day UV Protection Lotion

Composition % w/w INCI-Name (as supplied) Part A Glyceryl Stearate (and) PEG-100 5.00 Stearate Stearyl Alcohol 1.00 Tripalmitin 0.70 Dimethicone 2.00 Caprylic/Capric Triglyceride 5.00 Isopropyl Palmitate 5.00 Ethylhexyl Methoxycinnamate 3.00 Part B Water qs to 100 Polysorbate 60 0.50 Glycerin 3.00 Part C Water 10.00 UV-absorber dispersion as prepared 8.00 in example 6 Part D Phenoxyethanol (and) Methylparaben 0.70 (and) Ethylparaben (and) Butyl- paraben (and) Propylparaben (and) Isobutylparaben Steareth-10 Allyl Ether/Acrylates 1.50 Copolymer Part E Water (and) sodium hydroxide qs Part F Fragrance qs Preparation

Part A and B are heated separately up to 75° C.; part C to 60° C. Afterwards part B is poured into part A under stirring. The mixture is homogenized with an Ultra Turrax for 30 sec. at 11 000 rpm and part C is incorporated. After cooling down to 40° C. part D is added. At room temperature the pH-value is adjusted with Sodium Hydroxide between 6.30 and 6.70 and part F is added.

Example 22 Water Resistant Sunscreen Emulsion

Composition % w/w INCI-Name (as supplied) Part A Polyglyceryl-10 Pentastearate 2.50 (and) Behenyl Alcohol (and) Sodium Stearoyl Lactylate VP/Eicosene Copolymer 1.50 Stearyl Alcohol 1.50 Squalane 4.00 C₁₂₋₁₅ Alkyl Benzoate 7.50 Octocrylene 1.50 4-Methylbenzylidene Camphor 3.00 Ethylhexyl Methoxycinnamate 2.00 Part B Water qs to 100 Glycerin 1.80 Steareth-10 Allyl Ether/Acrylates Copolymer 0.80 Part C UV-absorber dispersion as prepared in example 6 9.00 Part D VP/Hexadecene Copolymer 2.70 Cyclomethicone 1.50 Phenoxyethanol (and) Methylparaben 0.70 (and) Ethylparaben (and) Butylparaben (and) Propylparaben (and) Isobutylparaben Part E Aqua (and) Tocopheryl Acetate 3.50 (and) Caprylic/Capric Triglyceride (and) Polysorbate 80 (and) Lecithin Part F Fragrance qs Water (and) sodium hydroxide qs Preparation

Part A and part B are heated separately to 80° C. Part A is poured into part B under continuous stirring. Afterwards the mixture is homogenized with an Ultra Turrax by 11 000 rpm for 1 min. After cooling down to 60° C. part C is incorporated. At 40° C. part D is added, and homogenized for a short time again. At 35° C. part E is added. Fragrance is added at room temperature. Finally the pH is adjusted with sodium hydroxide.

Example 23 UVA/UVB Sun Protection Lotion, O/W type

Composition % w/w INCI-Name (as supplied) Part A Potassium Cetyl Phosphate 2.00 Tricontanyl PVP 1.00 Caprylic/Capric Triglyceride 5.00 C₁₂₋₁₅ Alkyl Benzoate 5.00 Cetearyl Isononanoate 5.00 Glyceryl Stearate 3.00 Cetyl Alcohol 1.00 Dimethicone 0.10 Ethylhexyl Methoxycinnamate 5.00 Part B Water qs to 100 Glycerin 3.00 Part C Steareth-10 Allyl Ether/Acrylates Copolymer 0.50 Part D UV-absorber dispersion as prepared 8.00 in example 6 Part E Phenoxyethanol (and) Methylparaben 1.00 (and) Ethylparaben (and) Butylparaben (and) Propylparaben (and) Isobutylparaben Part F Water (and) Sodium Hydroxide qs to pH 7.00 Part G Fragrance qs Preparation

Part A and part B are heated separately up to 80° C. Part B is poured into part A under moderate stirring. The mixture is homogenized with an Ultra Turrax at 11000 rpm for 1 minute. After cooling down to 70° C. part C is added under stirring. After further cooling down to 50° C. part D is incorporated very slowly. At 40° C. part E is added. At room temperature the pH is adjusted with part F to 7.00 and part G is added.

Example 24 UVA/UVB Sun Protection Lotion, O/W type

Composition % w/w INCI-Name (as supplied) Part A Potassium Cetyl Phosphate 2.00 Tricontanyl PVP 1.00 Caprylic/Capric Triglyceride 5.00 C₁₂₋₁₅ Alkyl Benzoate 5.00 Cetearyl Isononanoate 5.00 Glyceryl Stearate 3.00 Cetyl Alcohol 1.00 Dimethicone 0.10 Ethylhexyl Methoxycinnamate 5.00 Part B Water qs to 100 Glycerin 3.00 Part C Steareth-10 Allyl Ether/Acrylates Copolymer 0.50 Part D UV-absorber dispersion as prepared 20.00  in example 6 Part E Phenoxyethanol (and) Methylparaben 1.00 (and) Ethylparaben (and) Butylparaben (and) Propylparaben (and) Isobutylparaben Part F Water (and) Sodium Hydroxide qs to pH 7.00 Part G Fragrance qs Preparation

Part A and part B are heated separately up to 80° C. Part B is poured into part A under moderate stirring. The mixture is homogenized with an Ultra Turrax at 11000 rpm for 1 minute. After cooling down to 70° C. part C is added under stirring. After further cooling down to 50° C. part D is incorporated very slowly. At 40° C. part E is added. At room temperature the pH is adjusted with part F to 7.00 and part G is added.

Example 25 Sunscreen Lotion

Composition % w/w INCI-Name (as supplied) Part A Cetearyl Alcohol (and) Dicetyl 4.00 Phosphate (and) Ceteth-10 Phosphate C₁₂₋₁₅ Alkyl Benzoate 2.00 Dicaprylyl Ether 3.00 Ethoxydiglycol Oleate 2.00 Stearic Acid 1.00 Ethylhexyl Methoxycinnamate 3.00 Sodium Acrylates Copolymer (and) 0.30 Glycine Soja (and) PPG-1 Trideceth-6 Squalane 3.50 VP/Eicosene Copolymer 2.00 Part B Water qs to 100 UV-absorber dispersion as prepared in example 6 5.00 Part C Diazolidinyl Urea (and) Iodopropynyl 0.15 Butylcarbamate Propylene Glycol 2.50 Water 10.00  Part D Cyclopentasiloxane (and) Dimethiconol 2.00 Ethoxydiglycol 5.00 Cyclopentasiloxane (and) Dimethicone/Vinyl 2.00 Dimethicone Crosspolymer Part E Aqua (and) Sodium Hydroxide qs Part F Fragrance qs Preparation

Part A and part B are heated separately up to 75° C. Part B is poured into part A under progressive stirring speed. Below 65° C. the ingredients of part D are added separately. After cooling down to 55° C. under moderate stirring part C is added. At a temperature below 35° C. the pH is checked and adjusted with Sodium Hydroxide and homogenized with an Ultra Turrax for 30 sec. at 11 000 rpm. At room temperature part F is added.

Example 26 W/O Sunscreen Lotion

Composition % w/w INCI-Name (as supplied) Part A PEG-7 Hydrogenated Castor Oil 3.00 Polyglyceryl-3 Diisostearate 4.00 Microcrystalline Wax 1.00 Magnesium Stearate 1.50 Propylparaben 0.10 Mineral Oil 15.00  Octyldodecanol 8.00 Ethylhexyl Triazone 1.00 Ethylhexyl Methoxycinnamate 2.00 Part B Water qs to 100 Water (and) Citric Acid 0.05 Methylparaben 0.15 Magnesium Sulfate 0.50 Part C UV-absorber dispersion as prepared in example 6 9.00 Fragrance qs Preparation

Part A is heated to 80° C. whilst stirring. Part B is added into part A and homogenized with an Ultra Turrax by 11 000 rpm for one minute. After cooling down to 30° C. part C is incorporated.

Example 27 Skin Protection Sunscreen Lotion W/O

Composition % w/w INCI-Name (as supplied) Part A Polyglyceryl-2 Dipolyhydroxystearate 3.00 Glyceryl Oleate 3.00 Cetearyl Isononanoate 7.00 Hexyl Laurate 6.00 Dicaprylyl Ether 6.00 Propylparaben 0.10 Hexyldecanol 3.00 Magnesium Stearate 1.00 Beeswax 1.00 Ethylhexyl Methoxycinnamate 4.00 Part B Water qs to 100 Methylparaben 0.15 Magnesium Sulfate 1.00 Part C UV-absorber dispersion as prepared in example 6 6.00 Preparation

Part A is heated separately to 80° C. under gentle stirring. Part B is added to part A and homogenized for one minute by 11000 rpm. After cooling down to 30° C. part C is added under continuous stirring. 

1. A UV absorber represented by compound of formula (1)

wherein R₁, R₂, R₃, R₄, R₅, R₆, R₇ and R₈ independently from each other are hydrogen; C₁-C₁₈alkyl; C₂-C₁₈alkenyl; C₅-C₇cycloalkyl or C₁-C₆alkylene-C₅-C₇cycloalkyl; R₉ is C₁-C₁₈alkyl; C₂-C₁₈alkenyl; C₅-C₇cycloalkyl; C₁-C₆alkylene-C₅-C₇cycloalkyl or C₆-C₁₀aryl; A is —S—; or —NR₁₀—, wherein R₁₀ is hydrogen, C₁-C₁₈alkyl; C₂-C₁₈alkenyl; C₅-C₇cycloalkyl; C₁-C₆alkylene-C₅-C₇cycloalkyl or C₆-C₁₀aryl; and X is COOR₁₁; CONR₁₂R₁₃; SO₃R₁₄ or SO₂NR₁₅R₁₆, wherein R₁₁, R₁₂, R₁₃, R₁₄, R₁₅ and R₁₆ are independently from each other hydrogen, C₁-C₁₈alkyl; C₂-C₁₈alkenyl; C₅-C₇cycloalkyl; C₁-C₆alkylene-C₅-C₇cycloalkyl or C₆-C₁₀aryl.
 2. A compound according to claim 1, wherein R₁, R₂, R₃, R₄, R₅, R₆, R₇ and R₈ independently from each other are hydrogen; C₁-C₁₀alkyl; C₂-C₁₀alkenyl; C₅-C₇cycloalkyl or C₁-C₄alkylene-C₅-C₇cycloalkyl; R₅ is hydrogen; C₁-C₁₀alkyl; C₂-C₁₀alkenyl; C₅-C₇cycloalkyl; C₁-C₄alkylene-C₅-C₇cycloalkyl; naphthyl or phenyl; A is —S—; or —NR₁₀—, wherein R₁₀ is hydrogen, C₁-C₁₈alkyl; C₂-C₁₈alkenyl; C₅-C₇cycloalkyl; C₁-C₆alkylene-C₅-C₇cycloalkyl or C₆-C₁₀aryl; and X is COOR₁₁; CONR₁₂R₁₃; SO₃R₁₄ or SO₂NR₁₅R₁₆, wherein R₁₁, R₁₂, R₁₃, R₁₄, R₁₅ and R₁₆ have independently from each other are hydrogen, C₁-C₁₈alkyl; C₂-C₁₈alkenyl; C₅-C₇cycloalkyl; C₁-C₆alkylene-C₅-C₇cycloalkyl or C₆-C₁₀aryl.
 3. A compound according to claim 1, wherein R₁, R₂, R₃, R₄, R₅, R₆, R₇ and R₈ are hydrogen.
 4. A compound according to claim 1, wherein R₁₁, R₁₂, R₁₃, R₁₄, R₁₅ and R₁₆ are hydrogen or C₁-C₁₂alkyl.
 5. A compound according to claim 1, wherein R₁, R₂, R₃, R₄, R₅, R₆, R₇, R₈, are hydrogen; and R₁₀, R₁₁, R₁₂, R₁₃, R₁₄, R₁₅ and R₁₆ are hydrogen or C₁-C₁₂alkyl.
 6. A compound according to claim 1 of formula (2)


7. A compound of formula (3)

R₉ is C₁-C₅alkyl; and R₁₇ is hydrogen; C₁-C₁₂alkyl or —NH₂.
 8. A process for the preparation of a compound of formula (1) according to claim 1, which process comprises reacting one mol of at least one compound of formula (4)

wherein Y is halogen; with at least two mols of at least one compound of formula (5)

where R₁, R₂, R₃, R₄, R₅, R₆, R₇ and R₈ independently from each other are hydrogen; C₁-C₁₈alkyl; C₂-C₁₈alkenyl; C₅-C₇cycloalkyl or C₁-C₆alkylene-C₅-C₇cycloalkyl; R₉ is C₁-C₁₈alkyl; C₂-C₁₈alkenyl; C₅-C₇cycloalkyl; C₁-C₆alkylene-C₅-C₇cycloalkyl or C₆-C₁₀aryl; A is —S—; or —NR₁₀—, wherein R₁₀ is hydrogen, C₁-C₁₈alkyl; C₂-C₁₈alkenyl; C₅-C₇cycloalkyl; C₁-C₆alkylene-C₅-C₇cycloalkyl or C₆-C₁₀aryl; and X is COOR₁₁; CONR₁₂R₁₃; SO₃R₁₄ or SO₂NR₁₅R₁₆, wherein R₁₁, R₁₂, R₁₃, R₁₄, R₁₅ and R₁₆ are independently hydrogen, C₁-C₁₈alkyl; C₂-C₁₈alkenyl; C₅-C₇cycloalkyl; C₁-C₆alkylene-C₅-C₇cycloalkyl or C₆-C₁₀aryl.
 9. A cosmetic preparation comprising at least one or more compounds of formula (1) according to claim 1 together with cosmetically tolerable carriers or adjuvants.
 10. A preparation according to claim 9 that further comprises in addition to the UV absorber of formula (1) further UV protective agents.
 11. A preparation according to claim 9 wherein the compound of formula (1) is in micronised form having an average particle size from 0.02 to 2 micrometers. 